Canonical Allele Identifier: PA308123
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1768Val
CA019094
NM_001099404.2:c.5302A>G