Canonical Allele Identifier: PA329998
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67810
ClinVar RCV Id: RCV000058585 RCV001262491 RCV001731355 RCV001842341 RCV004019048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1225Lys
CA017399
NM_001099404.2:c.3673G>A