Canonical Allele Identifier: PA2825491141
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1802Glu
CA352141178
NM_001099404.2:c.5406C>G
CA352141179
NM_001099404.2:c.5406C>A