Canonical Allele Identifier: PA2825129537
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2499691
ClinVar RCV Id: RCV003223783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp596Glu
CA352146158
NM_000335.5:c.1788C>G
CA352146160
NM_000335.5:c.1788C>A