Canonical Allele Identifier: PA2829973663
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_066399.2:p.Val534Gly
CA16615042
NM_021055.3:c.1601T>G