Allele Registry

Canonical Allele Identifier: PA2741913635

Gene: MED12 HGNC NCBI

ClinVar Variation Id: 2881453

HGVS (amino-acid)	Matching Registered Transcripts
NP_005111.2:p.Ser655Arg	CA413510189 NM_005120.3:c.1963A>C CA413510206 NM_005120.3:c.1965C>A CA413510208 NM_005120.3:c.1965C>G