Canonical Allele Identifier: PA2825185763
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374125
ClinVar RCV Id: RCV001877669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1221Thr
CA394292074
NM_000548.5:c.3661T>A