Canonical Allele Identifier: PA2825131206
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 265302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1308Cys
CA10588360
NM_000335.5:c.3922C>T