ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828180188
Gene: SCN9A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
195314
ClinVar RCV:
RCV000179414
RCV000192901
RCV000515449
RCV000540917
RCV001133337
RCV001133338
RCV001133339
RCV001195747
RCV002362922
ClinVar Variation:
198153
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001352465.1:p.Ile228Met
CA206037
NM_001365536.1:c.684C>G