Canonical Allele Identifier: PA2828420780
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Gln1460Pro
CA020573
NM_001370405.1:c.4379A>C