Canonical Allele Identifier: PA2827002061
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ala638Leu
CA658658369
NM_001318827.2:c.1912_1913delinsTT