Canonical Allele Identifier: PA265660
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Glu1574Lys
CA018503
NM_001099404.2:c.4720G>A