Canonical Allele Identifier: PA330185
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Pro1725Leu
CA018953
NM_001099404.2:c.5174C>T