Canonical Allele Identifier: PA2825489820
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1737895
ClinVar RCV Id: RCV002323385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1370Asn
CA352146941
NM_001099404.2:c.4108G>A