Canonical Allele Identifier: PA2829983603
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65291
ClinVar RCV Id: RCV000055513 RCV001814036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1700Leu
CA022229
NM_021055.3:c.5099G>T