Canonical Allele Identifier: PA2825490569
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919932
ClinVar RCV Id: RCV001566400 RCV002339446 RCV001842729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1609Leu
CA063800
NM_001099404.2:c.4826C>T