Allele Registry

Canonical Allele Identifier: PA216519

Gene: KRT12 HGNC NCBI

ClinVar RCV:

RCV000056428

RCV001730494

ClinVar Variation:

66128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000214.1:p.Pro15Ser	CA216518 NM_000223.4:c.43C>T