Canonical Allele Identifier: PA2827008337
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406089
ClinVar RCV Id: RCV000475335 RCV000761103 RCV002436402
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Asp921Gly
CA16615087
NM_001318829.2:c.2762A>G