Allele Registry

Canonical Allele Identifier: PA916009353

Gene: KRT8 HGNC NCBI

ClinVar RCV:

RCV000015735

RCV000056938

RCV002247346

ClinVar Variation:

14630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243211.1:p.Gly90Cys	CA124163 NM_001256282.2:c.268G>T