Canonical Allele Identifier: PA2825944731
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 579315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1189Glu
CA352149260
NM_001160161.2:c.3567C>G
CA352149262
NM_001160161.2:c.3567C>A