Canonical Allele Identifier: PA262989
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49896
ClinVar RCV Id: RCV000043163 RCV000478154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Cys244Arg
CA022889
NM_000548.5:c.730T>C