Canonical Allele Identifier: PA2825130999
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1691220
ClinVar RCV Id: RCV002254136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1217Ile
CA352137995
NM_000335.5:c.3650G>T