Canonical Allele Identifier: PA308080
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1325Ser
CA017686
NM_000335.5:c.3973G>T