Canonical Allele Identifier: PA2825942535
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ile1735Val
CA019094
NM_001160160.2:c.5203A>G