Canonical Allele Identifier: PA265871
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68001
ClinVar RCV Id: RCV000058795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Lys1871Asn
CA019389
NM_000335.5:c.5613G>C
CA352140620
NM_000335.5:c.5613G>T