Canonical Allele Identifier: PA2828416986
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala357Val
CA013675
NM_001370405.1:c.1070C>T