Canonical Allele Identifier: PA160394
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 134639
ClinVar RCV Id: RCV000121333 RCV003457641
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Arg438His
CA160393
NM_005120.3:c.1313G>A