Canonical Allele Identifier: PA2825942303
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1590Leu
CA018677
NM_001160160.2:c.4769G>T