Canonical Allele Identifier: PA2827007532
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gly622Asp
CA035599
NM_001318829.2:c.1865G>A