Canonical Allele Identifier: PA2825942556
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1331736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1747Gly
CA352141409
NM_001160160.2:c.5240A>G