Canonical Allele Identifier: PA2828098092
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350510.1:p.Ala384Val
CA3337185
NM_001363581.2:c.1151C>T