Canonical Allele Identifier: PA2827011019
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_001305758.1:p.Thr1618_Pro1622del
CA658656652
NM_001318829.2:c.4852_4866del