Canonical Allele Identifier: PA2829970256
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486639
ClinVar RCV Id: RCV000563255 RCV000644191
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly33Ser
CA056868
NM_021055.3:c.97G>A