Canonical Allele Identifier: PA265717
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gly1641Glu
CA018747
NM_000335.5:c.4922G>A