Canonical Allele Identifier: PA2827922895
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 242195
ClinVar RCV Id: RCV000231106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Gly1170Asp
CA10582192
NM_001354701.2:c.3509G>A