Allele Registry

Canonical Allele Identifier: PA915958918

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000056752

RCV003993782

ClinVar Variation:

66378

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Met272Thr	CA216980 NM_000526.5:c.815T>C