Canonical Allele Identifier: PA2826179872
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492
ClinVar RCV Id: RCV000193723 RCV001340866 RCV003430745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180277.1:p.Ala285Thr
CA207404
NM_001193348.1:c.853G>A