Canonical Allele Identifier: PA2829977312
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala894Val
CA040893
NM_021055.3:c.2681C>T