Canonical Allele Identifier: PA2827008157
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala845Val
CA040893
NM_001318829.2:c.2534C>T