Canonical Allele Identifier: PA2827922307
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 379063
ClinVar RCV Id: RCV000432154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Met794Thr
CA16604918
NM_001354701.2:c.2381T>C