Canonical Allele Identifier: PA2825939931
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 921391
ClinVar RCV Id: RCV001564789 RCV001843075 RCV002327435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg15Gly
CA056713
NM_001160160.2:c.43A>G