Canonical Allele Identifier: PA2828415456
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 578447
ClinVar RCV Id: RCV000701459 RCV002334351 RCV002493231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1678Val
CA394313865
NM_001370404.1:c.5033C>T