Canonical Allele Identifier: PA2826179841
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 589526
ClinVar RCV Id: RCV002316756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180277.1:p.Met219Thr
CA360423169
NM_001193348.1:c.656T>C