Canonical Allele Identifier: PA2829975888
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu733Val
CA016903
NM_021055.3:c.2197C>G