Allele Registry

Canonical Allele Identifier: PA915958845

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015724

RCV000056709

ClinVar Variation:

14620

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Met119Ile	CA216903 NM_000526.5:c.357G>A CA399482581 NM_000526.5:c.357G>T CA399482582 NM_000526.5:c.357G>C