Allele Registry

Canonical Allele Identifier: PA915958935

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015715

RCV000056667

RCV003387723

ClinVar Variation:

14611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Leu384Pro	CA216827 NM_000526.5:c.1151T>C