Canonical Allele Identifier: PA2828421195
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala1574Val
CA394308216
NM_001370405.1:c.4721C>T