Canonical Allele Identifier: PA2828095367
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala1676Val
CA394314530
NM_001363528.2:c.5027C>T