Canonical Allele Identifier: PA2825494011
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu673Pro
CA015742
NM_001099405.2:c.2018T>C