Canonical Allele Identifier: PA2827010448
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Lys1633Thr
CA394314672
NM_001318829.2:c.4898A>C