Canonical Allele Identifier: PA2825491654
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1980Phe
CA065024
NM_001099404.2:c.5938G>T