Allele Registry

Canonical Allele Identifier: PA100070

Gene: MED12 HGNC NCBI

ClinVar RCV:

RCV000012276

RCV000415294

RCV000763632

RCV001261368

RCV001330015

RCV001528259

RCV003764560

RCV004018614

ClinVar Variation:

11520

HGVS (amino-acid)	Matching Registered Transcripts
NP_005111.2:p.Arg961Trp	CA324786 NM_005120.3:c.2881C>T