Canonical Allele Identifier: PA2825491087
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1331736
ClinVar RCV Id: RCV001842163 RCV003542347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1780Gly
CA352141409
NM_001099404.2:c.5339A>G