Canonical Allele Identifier: PA307247
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val411Met
CA014560
NM_000335.5:c.1231G>A