Canonical Allele Identifier: PA2828414768
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_001357333.1:p.Asp1491Ala
CA020755
NM_001370404.1:c.4472A>C