Allele Registry

Canonical Allele Identifier: PA915958851

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015723

RCV000056708

ClinVar Variation:

14619

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Met119Thr	CA216901 NM_000526.5:c.356T>C