Canonical Allele Identifier: PA2827020951
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1686Val
CA394314530
NM_001318832.2:c.5057C>T