Canonical Allele Identifier: PA2825439546
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1675Val
CA394314530
NM_001077183.3:c.5024C>T