Canonical Allele Identifier: PA2827018335
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564684
ClinVar RCV Id: RCV003297116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser890Thr
CA394278477
NM_001318832.2:c.2668T>A