Canonical Allele Identifier: PA2825132828
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3069459
ClinVar RCV Id: RCV004008003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1965Pro
CA352139533
NM_000335.5:c.5893T>C