Canonical Allele Identifier: PA2828412921
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207738
ClinVar RCV Id: RCV000231299 RCV000561234 RCV001705073 RCV003996891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr952Ala
CA043628
NM_001370404.1:c.2854A>G