Canonical Allele Identifier: PA2827005155
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys1555Arg
CA16615040
NM_001318827.2:c.4664A>G