Canonical Allele Identifier: PA2827010401
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 661952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1620Thr
CA276759442
NM_001318829.2:c.4859T>C