Canonical Allele Identifier: PA916023980
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala905Val
CA040893
NM_001318832.2:c.2714C>T