Canonical Allele Identifier: PA645415543
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 225253
ClinVar RCV Id: RCV000416709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Arg621Gln
CA16044154
NM_005120.3:c.1862G>A