Canonical Allele Identifier: PA2825497096
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met1775Lys
CA019186
NM_001099405.2:c.5324T>A