Canonical Allele Identifier: PA2825537721
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 578662
ClinVar RCV Id: RCV002507225 RCV003655202 RCV003999719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly298Asp
CA065869
NM_001099404.2:c.893G>A