Canonical Allele Identifier: PA2827007524
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2825177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro620Thr
CA394274455
NM_001318829.2:c.1858C>A