Allele Registry

Canonical Allele Identifier: PA915958858

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056712

ClinVar Variation:

66344

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Leu122Phe	CA216909 NM_000526.5:c.364C>T