Canonical Allele Identifier: PA2825129565
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 570937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asp608Asn
CA058871
NM_000335.5:c.1822G>A