Canonical Allele Identifier: PA2825942740
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg1864Trp
CA353758
NM_001160160.2:c.5590C>T