Canonical Allele Identifier: PA216519
Gene: KRT12 HGNC NCBI

Linked Data

ClinVar Variation Id: 66128
ClinVar RCV Id: RCV000056428 RCV001730494
JSON-LD

Amino-acid Alleles

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