Canonical Allele Identifier: PA2828089680
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Lys34Arg
CA027990
NM_001363528.2:c.101A>G