Canonical Allele Identifier: PA263163
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1438Gln
CA020250
NM_000548.5:c.4313G>A