Canonical Allele Identifier: PA2827020563
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp1588Asn
CA053097
NM_001318832.2:c.4762G>A