Canonical Allele Identifier: PA2828092213
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318320
ClinVar RCV Id: RCV000309089 RCV000644137 RCV002446569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr771Ile
CA10637328
NM_001363528.2:c.2312C>T