RUNX2 c.36A>C ;(p.P12=)

Variant ID: 6-45296499-A-C

NM_001024630.3(RUNX2):c.36A>C;(p.P12=)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A fibronectin peptide redirects PDGF-BB/PDGFR complexes to macropinocytosis-like internalization and augments PDGF-BB survival signals.

The Journal Of Investigative Dermatology
Zhu, Jia J; Lin, Fubao F; Brown, Deborah A DA; Clark, Richard A F RAF
Publication Date: 2014-04

Variant appearance in text: CCD: P12=
PubMed Link: 24304816
Variant Present in the following documents:
  • Main text
View BVdb publication page