ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828180596
Gene: SCN9A
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000006738
RCV000557785
RCV001535456
RCV002408454
ClinVar Variation:
6366
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001352465.1:p.Asn641Tyr
CA118164
NM_001365536.1:c.1921A>T