Canonical Allele Identifier: PA2825577547
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_001107854.1:p.Thr1710_Pro1714del
CA658656652
NM_001114382.3:c.5128_5142del