Canonical Allele Identifier: PA2825945597
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1739Lys
CA019186
NM_001160161.2:c.5216T>A