Canonical Allele Identifier: PA2825942946
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 840267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1976Glu
CA065218
NM_001160160.2:c.5928C>G
CA352139043
NM_001160160.2:c.5928C>A