Canonical Allele Identifier: PA658681363
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_000539.2:p.Thr1733_Pro1737del
CA658656652
NM_000548.5:c.5197_5211del