Canonical Allele Identifier: PA330106
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1503Pro
CA018376
NM_001099404.2:c.4507T>C