Canonical Allele Identifier: PA2828180188
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 198153
ClinVar RCV Id: RCV000179414 RCV000192901 RCV000515449 RCV000540917 RCV001133337 RCV001133338 RCV001133339 RCV001195747 RCV002362922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile228Met
CA206037
NM_001365536.1:c.684C>G