Canonical Allele Identifier: PA2827010717
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr1370Ile
CA051214
NM_001318829.2:c.4109C>T