Canonical Allele Identifier: PA2827922049
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 570937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp608Asn
CA058871
NM_001354701.2:c.1822G>A