Canonical Allele Identifier: PA2825491646
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 963939
ClinVar RCV Id: RCV003656727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1976Ala
CA352139436
NM_001099404.2:c.5926T>G