Canonical Allele Identifier: PA2825132709
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1918His
CA064762
NM_000335.5:c.5753G>A