Canonical Allele Identifier: PA2827005539
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gln1649Glu
CA394314782
NM_001318827.2:c.4945C>G