Canonical Allele Identifier: PA1139742843
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 952898
ClinVar RCV Id: RCV001225099 RCV002436875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile990Val
CA349074657
NM_001365536.1:c.2968A>G