Canonical Allele Identifier: PA2827923540
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743446
ClinVar RCV Id: RCV002330776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ile1592Thr
CA352143135
NM_001354701.2:c.4775T>C