Allele Registry

Canonical Allele Identifier: PA915958961

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056677

ClinVar Variation:

66314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Glu411Lys	CA216846 NM_000526.5:c.1231G>A