Canonical Allele Identifier: PA2828421716
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406068
ClinVar RCV Id: RCV000572414 RCV000589806 RCV001086420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile1707Met
CA054841
NM_001370405.1:c.5121C>G