Canonical Allele Identifier: PA162622
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135388
ClinVar RCV Id: RCV000122237 RCV000706466 RCV001022523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala1489Thr
CA020493
NM_000548.5:c.4465G>A