Canonical Allele Identifier: PA2828094135
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1343Gly
CA276753368
NM_001363528.2:c.4027C>G