Canonical Allele Identifier: PA2825940278
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532103
ClinVar RCV Id: RCV001841840 RCV003539998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ser262Gly
CA065668
NM_001160160.2:c.784A>G