Canonical Allele Identifier: PA2827923524
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 658093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ile1584Phe
CA352143580
NM_001354701.2:c.4750A>T