Allele Registry

Canonical Allele Identifier: PA915958977

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056689

ClinVar Variation:

66325

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg417Pro	CA216868 NM_000526.5:c.1250G>C