Canonical Allele Identifier: PA2825130419
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3075097
ClinVar RCV Id: RCV004015623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Thr1007Asn
CA72926298
NM_000335.5:c.3020C>A