Canonical Allele Identifier: PA2825132604
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1874dup
CA542615522
NM_000335.5:c.5620_5622dup