Canonical Allele Identifier: PA2825940998
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu737Lys
CA015965
NM_001160160.2:c.2209G>A