Canonical Allele Identifier: PA2825945583
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Leu1732Gln
CA019153
NM_001160161.2:c.5195T>A