Canonical Allele Identifier: PA916023011
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486673
ClinVar RCV Id: RCV000562552 RCV001853809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Lys862Met
CA045694
NM_001318831.2:c.2585A>T