Canonical Allele Identifier: PA2825130243
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1034782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asn932Ser
CA352140794
NM_000335.5:c.2795A>G