Canonical Allele Identifier: PA1139742838
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 961015
ClinVar RCV Id: RCV001234644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ala939Val
CA349077184
NM_001365536.1:c.2816C>T