Canonical Allele Identifier: PA2828095235
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421466
ClinVar RCV Id: RCV000483888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg1647_Ala1650del
CA16620104
NM_001363528.2:c.4940_4951del