Canonical Allele Identifier: PA329814
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg53Gln
CA015041
NM_000335.5:c.158G>A