Canonical Allele Identifier: PA2828418726
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Leu850Pro
CA017661
NM_001370405.1:c.2549T>C