Canonical Allele Identifier: PA330184
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro1724Leu
CA018953
NM_000335.5:c.5171C>T