Canonical Allele Identifier: PA2825490538
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 658093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ile1603Phe
CA352143580
NM_001099404.2:c.4807A>T