Canonical Allele Identifier: PA2825538807
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2189234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1190Phe
CA352138191
NM_001099404.2:c.3568G>T