Canonical Allele Identifier: PA307882
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201542
ClinVar RCV Id: RCV000183129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1876Lys
CA019400
NM_001099404.2:c.5626G>A