Canonical Allele Identifier: PA2827924076
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 978333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1919Asp
CA352139848
NM_001354701.2:c.5757A>T
CA352139850
NM_001354701.2:c.5757A>C