Canonical Allele Identifier: PA2827923820
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 836588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1762Gly
CA352141392
NM_001354701.2:c.5285A>G