Canonical Allele Identifier: PA2827019587
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1313Gln
CA019956
NM_001318832.2:c.3938G>A