Canonical Allele Identifier: PA2825132952
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 840267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp2008Glu
CA065218
NM_000335.5:c.6024C>G
CA352139043
NM_000335.5:c.6024C>A