Allele Registry

Canonical Allele Identifier: PA2826381032

Gene: KRT8 HGNC NCBI

ClinVar RCV:

RCV000015737

RCV000056936

RCV000988859

RCV001777139

ClinVar Variation:

14631

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243222.1:p.Tyr54His	CA124165 NM_001256293.2:c.160T>C