Canonical Allele Identifier: PA2828410005
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65223
ClinVar RCV Id: RCV000055443 RCV000573567 RCV000989413 RCV001555447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg98Trp
CA018319
NM_001370404.1:c.292C>T