Canonical Allele Identifier: PA2825944527
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asp1062Glu
CA352139112
NM_001160161.2:c.3186T>G
CA352139114
NM_001160161.2:c.3186T>A