Allele Registry

Canonical Allele Identifier: PA130790

Gene: MEF2C HGNC NCBI

ClinVar RCV:

RCV000033231

ClinVar Variation:

40216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124477.1:p.Gly27Ala	CA130789 NM_001131005.2:c.80G>C