CCT5 c.1615T>G ;(p.S539A)

Variant ID: 5-10264884-T-G

NM_012073.3(CCT5):c.1615T>G;(p.S539A)

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: