Allele Registry

Canonical Allele Identifier: PA915958978

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056690

ClinVar Variation:

66326

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Leu418Val	CA216870 NM_000526.5:c.1252C>G