CCT5 c.1613A>C ;(p.E538A)

Variant ID: 5-10264882-A-C

NM_012073.3(CCT5):c.1613A>C;(p.E538A)

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: