Canonical Allele Identifier: PA2825497052
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_001092875.1:p.Glu1762Gly
CA352141409
NM_001099405.2:c.5285A>G