ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829983566
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001023747
RCV001061035
RCV001772198
RCV004004640
ClinVar Variation:
825558
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Trp1697Ser
CA394314459
NM_021055.3:c.5090G>C