Canonical Allele Identifier: PA2829970206
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg25Lys
CA056318
NM_021055.3:c.74G>A