Canonical Allele Identifier: PA2825132582
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1479679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1863Gly
CA352140722
NM_000335.5:c.5588A>G