Canonical Allele Identifier: PA2828421662
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1695Val
CA394314530
NM_001370405.1:c.5084C>T