Canonical Allele Identifier: PA2825538766
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 926342
ClinVar RCV Id: RCV001841060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1158Val
CA352138401
NM_001099404.2:c.3473G>T