Canonical Allele Identifier: PA658805095
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535941
ClinVar RCV Id: RCV000644175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Tyr1571His
CA394307381
NM_000548.5:c.4711T>C