Canonical Allele Identifier: PA916023753
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala686Thr
CA10583300
NM_001318832.2:c.2056G>A