Canonical Allele Identifier: PA2828095408
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gln1686Glu
CA394314782
NM_001363528.2:c.5056C>G