Allele Registry

Canonical Allele Identifier: PA915958854

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056710

ClinVar Variation:

66342

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Gln120Pro	CA216905 NM_000526.5:c.359A>C