Canonical Allele Identifier: PA2827008040
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu801Pro
CA017661
NM_001318829.2:c.2402T>C