Canonical Allele Identifier: PA2827923857
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 628960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp1783Glu
CA352141178
NM_001354701.2:c.5349C>G
CA352141179
NM_001354701.2:c.5349C>A