Canonical Allele Identifier: PA2573199466
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala53Val
CA276768623
NM_001318832.2:c.158C>T