Allele Registry

Canonical Allele Identifier: PA915958917

Gene: KRT14 HGNC NCBI

ClinVar RCV:

RCV000015721

RCV000056753

ClinVar Variation:

14617

HGVS (amino-acid)	Matching Registered Transcripts
NP_000517.3:p.Met272Arg	CA216982 NM_000526.5:c.815T>G