Canonical Allele Identifier: PA330191
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1739Trp
CA018994
NM_001099404.2:c.5215C>T