Canonical Allele Identifier: PA2825131787
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774439
ClinVar RCV Id: RCV003592322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ile1569Thr
CA352143792
NM_000335.5:c.4706T>C