Canonical Allele Identifier: PA2827010400
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468147
ClinVar Variation Id: 2806460
ClinVar RCV Id: RCV003627753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1620Val
CA054409
NM_001318829.2:c.4858A>G
CA2739269936
NM_001318829.2:c.4857_4858delinsCG