Allele Registry

Canonical Allele Identifier: PA915958974

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056685

RCV001731185

ClinVar Variation:

14621

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Tyr415His	CA216861 NM_000526.5:c.1243T>C