Canonical Allele Identifier: PA2825436144
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly671Asp
CA035599
NM_001077183.3:c.2012G>A