Canonical Allele Identifier: PA2825131194
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 926452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1305Cys
CA352148144
NM_000335.5:c.3913C>T