Canonical Allele Identifier: PA2828089701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141455
ClinVar RCV Id: RCV000129975 RCV003626606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile40Thr
CA014027
NM_001363528.2:c.119T>C