Canonical Allele Identifier: PA2827010420
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1627Val
CA394314530
NM_001318829.2:c.4880C>T