Canonical Allele Identifier: PA645415614
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 374138
ClinVar RCV Id: RCV000415054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Gly1448Arg
CA16043598
NM_005120.3:c.4342G>A
CA413526493
NM_005120.3:c.4342G>C