Canonical Allele Identifier: PA2829981704
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65219
ClinVar RCV Id: RCV000055439
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp1492Ala
CA020755
NM_021055.3:c.4475A>C