Canonical Allele Identifier: PA307852
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1793Lys
CA019186
NM_001099404.2:c.5378T>A