Canonical Allele Identifier: PA2573170594
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala1742Val
CA394314530
NM_000548.5:c.5225C>T