Canonical Allele Identifier: PA2828180358
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471079
ClinVar RCV Id: RCV000553821 RCV002527904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala402Thr
CA1944569
NM_001365536.1:c.1204G>A