ClinGen Allele Registry
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Canonical Allele Identifier:
PA916023813
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000042858
RCV000129683
RCV000227547
RCV001703935
ClinVar Variation:
49597
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305761.1:p.Arg729Pro
CA016844
NM_001318832.2:c.2186G>C