CCT5 c.1606C>G ;(p.P536A)

Variant ID: 5-10264875-C-G

NM_012073.3(CCT5):c.1606C>G;(p.P536A)

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: