Allele Registry

Canonical Allele Identifier: PA915958862

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056716

ClinVar Variation:

66347

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg125Gly	CA216917 NM_000526.5:c.373C>G