Canonical Allele Identifier: PA2828095159
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Met1625Thr
CA021670
NM_001363528.2:c.4874T>C