Allele Registry

Canonical Allele Identifier: PA2826180165

Gene: MEF2C HGNC NCBI

ClinVar RCV:

RCV000479668

ClinVar Variation:

424592

HGVS (amino-acid)	Matching Registered Transcripts
NP_001180278.1:p.Arg321Cys	CA16618217 NM_001193349.2:c.961C>T