Canonical Allele Identifier: PA2829205629
Gene: MEF2A HGNC NCBI

Linked Data

ClinVar Variation Id: 8949
ClinVar RCV Id: RCV000009505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001380488.1:p.Pro209Leu
CA120015
NM_001393559.2:c.626C>T