Canonical Allele Identifier: PA2825940415
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67629
ClinVar RCV Id: RCV000058385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Gly351Asp
CA014239
NM_001160160.2:c.1052G>A