Canonical Allele Identifier: PA216521
Gene: KRT12 HGNC NCBI

Linked Data

ClinVar Variation Id: 66129
ClinVar RCV Id: RCV000056429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000214.1:p.Arg19Trp
CA216520
NM_000223.4:c.55C>T