Canonical Allele Identifier: PA2827008181
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro854Thr
CA394279461
NM_001318829.2:c.2560C>A