Canonical Allele Identifier: PA2828411983
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486625
ClinVar RCV Id: RCV000566288 RCV000693999 RCV001840684 RCV004001151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly676Val
CA035845
NM_001370404.1:c.2027G>T