Canonical Allele Identifier: PA265442
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67858
ClinVar RCV Id: RCV000058637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1358Trp
CA017852
NM_001099404.2:c.4072G>T