Allele Registry

Canonical Allele Identifier: PA915958979

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015727

RCV000056691

ClinVar Variation:

14622

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Leu419Gln	CA216872 NM_000526.5:c.1256T>A