Canonical Allele Identifier: PA2827016757
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230395
ClinVar RCV Id: RCV000213113 RCV000537615
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser17Asn
CA033570
NM_001318832.2:c.50G>A