Canonical Allele Identifier: PA2828420599
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49830
ClinVar RCV Id: RCV000043096 RCV001050539 RCV001022358
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1411Gly
CA020332
NM_001370405.1:c.4231A>G