Canonical Allele Identifier: PA916022822
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238013
ClinVar RCV Id: RCV000228906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu972Pro
CA10583318
NM_001318827.2:c.2915T>C