Canonical Allele Identifier: PA2827922946
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1484935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1201Met
CA72923192
NM_001354701.2:c.3601G>A