Canonical Allele Identifier: PA2829981794
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64985
ClinVar RCV Id: RCV000055189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1504Gly
CA020797
NM_021055.3:c.4511T>G