Canonical Allele Identifier: PA2827008872
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497442
ClinVar RCV Id: RCV003213897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1135_Leu1136del
CA2580091013
NM_001318829.2:c.3404_3409del