Canonical Allele Identifier: PA2827015583
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp1268Asn
CA16614792
NM_001318831.2:c.3802G>A