Allele Registry

Canonical Allele Identifier: PA915958883

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056727

ClinVar Variation:

66356

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Val133Met	CA216937 NM_000526.5:c.397G>A