Canonical Allele Identifier: PA2825130798
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309424
ClinVar RCV Id: RCV001765593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1134Thr
CA352138548
NM_000335.5:c.3401G>C