Canonical Allele Identifier: PA2828419160
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386865
ClinVar RCV Id: RCV000433002 RCV000456443 RCV002323631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Met987Val
CA044156
NM_001370405.1:c.2959A>G