Allele Registry

Canonical Allele Identifier: PA915990342

Gene: MEF2C HGNC NCBI

ClinVar RCV:

RCV000223956

ClinVar Variation:

218315

HGVS (amino-acid)	Matching Registered Transcripts
NP_002388.2:p.Arg3Ser	CA10575830 NM_002397.5:c.9A>T CA360425353 NM_002397.5:c.9A>C