Canonical Allele Identifier: PA307758
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201526
ClinVar RCV Id: RCV000183097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met1676Thr
CA018860
NM_001099404.2:c.5027T>C