Canonical Allele Identifier: PA916023037
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64927
ClinVar RCV Id: RCV000055129 RCV000465863 RCV001020133 RCV001697040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp882Val
CA019052
NM_001318831.2:c.2645A>T