Canonical Allele Identifier: PA2826179844
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 438583
ClinVar RCV Id: RCV000656084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180277.1:p.Ser231Leu
CA3337223
NM_001193348.1:c.692C>T