Canonical Allele Identifier: PA658681192
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1409Gly
CA276753368
NM_000548.5:c.4225C>G