Canonical Allele Identifier: PA2825945610
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1748Glu
CA352141178
NM_001160161.2:c.5244C>G
CA352141179
NM_001160161.2:c.5244C>A