Canonical Allele Identifier: PA2825495370
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg1175Cys
CA017218
NM_001099405.2:c.3523C>T