Canonical Allele Identifier: PA2825942179
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ser1502Pro
CA018376
NM_001160160.2:c.4504T>C