Canonical Allele Identifier: PA2825489781
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 660890
ClinVar RCV Id: RCV003539339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1358Glu
CA352147155
NM_001099404.2:c.4073G>A