ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829977995
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000475335
RCV000761103
RCV002436402
ClinVar Variation:
406089
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Asp970Gly
CA16615087
NM_021055.3:c.2909A>G