Canonical Allele Identifier: PA2825575850
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497442
ClinVar RCV Id: RCV003213897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1227_Leu1228del
CA2580091013
NM_001114382.3:c.3680_3685del