Canonical Allele Identifier: PA2825497122
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp1784Glu
CA352141178
NM_001099405.2:c.5352C>G
CA352141179
NM_001099405.2:c.5352C>A