Canonical Allele Identifier: PA2827005551
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1651Met
CA054841
NM_001318827.2:c.4953C>G