Canonical Allele Identifier: PA2825571949
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr41Ala
CA394301694
NM_001114382.3:c.121A>G