Canonical Allele Identifier: PA916045272
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 572510
ClinVar RCV Id: RCV000693906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val741Gly
CA349079687
NM_001365536.1:c.2222T>G