Canonical Allele Identifier: PA2825491582
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1958Leu
CA352139611
NM_001099404.2:c.5873G>T