Canonical Allele Identifier: PA319848
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 213627
ClinVar RCV Id: RCV000766104 RCV001721275 RCV002354550 RCV003985305 RCV003595887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Met2033Val
CA319847
NM_005120.3:c.6097A>G