Canonical Allele Identifier: PA2825495450
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1484935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1202Met
CA72923192
NM_001099405.2:c.3604G>A