Allele Registry

Canonical Allele Identifier: PA112550

Gene: KRT8 HGNC NCBI

ClinVar RCV:

RCV000015735

RCV000056938

RCV002247346

ClinVar Variation:

14630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243222.1:p.Gly62Cys	CA124163 NM_001256293.2:c.184G>T