ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828180495
Gene: SCN9A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
283355
ClinVar RCV:
RCV000293514
RCV000346132
RCV000363472
RCV000401490
RCV000493503
RCV000688718
ClinVar Variation:
331988
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001352465.1:p.Arg540His
CA1944463
NM_001365536.1:c.1619G>A