Canonical Allele Identifier: PA658806011
Gene: MED12 HGNC NCBI

Linked Data

ClinVar Variation Id: 522111
ClinVar RCV Id: RCV000623246 RCV001580299 RCV001805226 RCV003117433 RCV003596075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005111.2:p.Arg296Gln
CA413504438
NM_005120.3:c.887G>A