ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828180201
Gene: SCN9A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
6351
ClinVar RCV Id:
RCV000006723
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001352465.1:p.Ser241Thr
CA340548
NM_001365536.1:c.721T>A