Canonical Allele Identifier: PA308110
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1497Thr
CA018346
NM_000335.5:c.4490T>C