Canonical Allele Identifier: PA2825537733
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 960705
ClinVar RCV Id: RCV003656705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu306Ile
CA352150351
NM_001099404.2:c.916C>A