Canonical Allele Identifier: PA916023750
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala684Val
CA035710
NM_001318832.2:c.2051C>T