Canonical Allele Identifier: PA2828089706
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Thr41Ala
CA394301694
NM_001363528.2:c.121A>G