Canonical Allele Identifier: PA2827020271
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1504Thr
CA052272
NM_001318832.2:c.4510G>A