Canonical Allele Identifier: PA307249
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val411Met
CA014560
NM_001160161.2:c.1231G>A