Canonical Allele Identifier: PA2825131868
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 658093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1602Phe
CA352143580
NM_000335.5:c.4804A>T