Canonical Allele Identifier: PA330209
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67973
ClinVar RCV Id: RCV000058759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1761His
CA019056
NM_001099404.2:c.5282T>A