Canonical Allele Identifier: PA2828420889
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061534
ClinVar RCV Id: RCV001371130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Val1488Ala
CA394304503
NM_001370405.1:c.4463T>C