Canonical Allele Identifier: PA2828421639
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226
ClinVar RCV Id: RCV003106975 RCV003384352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Tyr1689Cys
CA394314314
NM_001370405.1:c.5066A>G