Canonical Allele Identifier: PA2825131860
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3073613
ClinVar RCV Id: RCV004016619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1598Leu
CA352143606
NM_000335.5:c.4792G>C