Canonical Allele Identifier: PA2826180165
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 424592
ClinVar RCV Id: RCV000479668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180278.1:p.Arg321Cys
CA16618217
NM_001193349.2:c.961C>T