Canonical Allele Identifier: PA2827921289
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070624
ClinVar RCV Id: RCV004013134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu83Met
CA352157897
NM_001354701.2:c.247C>A