Canonical Allele Identifier: PA2827923975
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Glu1857Val
CA352140568
NM_001354701.2:c.5570A>T