Canonical Allele Identifier: PA2825130952
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1484935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1201Met
CA72923192
NM_000335.5:c.3601G>A