Canonical Allele Identifier: PA2827017985
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2825177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro680Thr
CA394274455
NM_001318832.2:c.2038C>A