Canonical Allele Identifier: PA916056654
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65223
ClinVar RCV Id: RCV000055443 RCV000573567 RCV000989413 RCV001555447
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg98Trp
CA018319
NM_021055.3:c.292C>T