Canonical Allele Identifier: PA2825496433
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_001092875.1:p.Ile1552Thr
CA352143792
NM_001099405.2:c.4655T>C