Canonical Allele Identifier: PA2825130609
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Glu1072del
CA061383
NM_000335.5:c.3214_3216del