Canonical Allele Identifier: PA2825489760
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1355Pro
CA352147218
NM_001099404.2:c.4064T>C