Canonical Allele Identifier: PA2825538140
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1043347

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Cys649Arg
CA059318
NM_001099404.2:c.1945T>C