Canonical Allele Identifier: PA2827009360
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Asp1291Asn
CA050657
NM_001318829.2:c.3871G>A