Canonical Allele Identifier: PA916023767
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237977
ClinVar RCV Id: RCV000226719 RCV001014169
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu692Gln
CA10583301
NM_001318832.2:c.2075T>A