Canonical Allele Identifier: PA2825128211
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1172409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro52His
CA056571
NM_000335.5:c.155C>A