Canonical Allele Identifier: PA2827008902
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 383442
ClinVar RCV Id: RCV001020951 RCV000964609 RCV001703809 RCV004533019 RCV003235210
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1145Val
CA048133
NM_001318829.2:c.3434C>T