Canonical Allele Identifier: PA2825940661
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1002978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Lys521Glu
CA058165
NM_001160160.2:c.1561A>G