Canonical Allele Identifier: PA2828095329
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486668
ClinVar RCV Id: RCV000565556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr1667_Pro1671del
CA658656652
NM_001363528.2:c.4999_5013del