Canonical Allele Identifier: PA2827016416
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ile1491Thr
CA276759442
NM_001318831.2:c.4472T>C