Canonical Allele Identifier: PA2827020203
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051582
ClinVar RCV Id: RCV001359645 RCV004036738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Thr1486Ile
CA394304843
NM_001318832.2:c.4457C>T