Canonical Allele Identifier: PA2827020981
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Lys1692Thr
CA394314672
NM_001318832.2:c.5075A>C