Canonical Allele Identifier: PA2826180101
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1310329
ClinVar RCV Id: RCV001767443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180278.1:p.Arg203His
CA360423273
NM_001193349.2:c.608G>A