Canonical Allele Identifier: PA2829983161
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49350
ClinVar RCV Id: RCV000042610 RCV000517378
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1666Arg
CA021789
NM_021055.3:c.4997C>G