Canonical Allele Identifier: PA2825131806
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1045161
ClinVar RCV Id: RCV003656913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1576Ile
CA352143746
NM_000335.5:c.4726G>A