Canonical Allele Identifier: PA2825132606
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1875Val
CA352140568
NM_000335.5:c.5624A>T