Canonical Allele Identifier: PA2826180099
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1720584
ClinVar RCV Id: RCV002298302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180278.1:p.Asn201Ser
CA360423288
NM_001193349.2:c.602A>G