Canonical Allele Identifier: PA2828411421
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406006
ClinVar RCV Id: RCV000571306 RCV000460751 RCV004000693 RCV003470408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val534Gly
CA16615042
NM_001370404.1:c.1601T>G