Canonical Allele Identifier: PA2828420902
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65219
ClinVar RCV Id: RCV000055439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1492Ala
CA020755
NM_001370405.1:c.4475A>C