Canonical Allele Identifier: PA264721
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65328
ClinVar RCV Id: RCV000055552 RCV000494277 RCV000660343 RCV002415509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val705Met
CA016792
NM_000548.5:c.2113G>A