Canonical Allele Identifier: PA2825132369
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1331736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1779Gly
CA352141409
NM_000335.5:c.5336A>G