Canonical Allele Identifier: PA265966
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val300Ile
CA019931
NM_001099404.2:c.898G>A