Canonical Allele Identifier: PA2827010765
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64985
ClinVar RCV Id: RCV000055189
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val1432Gly
CA020797
NM_001318829.2:c.4295T>G