Canonical Allele Identifier: PA2828091656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala623Val
CA16608037
NM_001363528.2:c.1868C>T