Canonical Allele Identifier: PA2825940928
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Cys683Gly
CA015785
NM_001160160.2:c.2047T>G