Canonical Allele Identifier: PA2825945755
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1843Trp
CA353758
NM_001160161.2:c.5527C>T