Allele Registry

Canonical Allele Identifier: PA915958976

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056688

ClinVar Variation:

66324

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Arg416Pro	CA216866 NM_000526.5:c.1247G>C