Canonical Allele Identifier: PA2825942562
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1751Lys
CA019148
NM_001160160.2:c.5251G>A