Allele Registry

Canonical Allele Identifier: PA916009351

Gene: KRT8 HGNC NCBI

ClinVar RCV:

RCV000015737

RCV000056936

RCV000988859

RCV001777139

ClinVar Variation:

14631

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243211.1:p.Tyr82His	CA124165 NM_001256282.2:c.244T>C