Canonical Allele Identifier: PA2825184769
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073959
ClinVar RCV Id: RCV004012501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Thr1075Pro
CA394285967
NM_000548.5:c.3223A>C