Canonical Allele Identifier: PA2825132803
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1957Leu
CA352139611
NM_000335.5:c.5870G>T