Canonical Allele Identifier: PA2825576796
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_001107854.1:p.Val1508Ala
CA394304503
NM_001114382.3:c.4523T>C