Canonical Allele Identifier: PA2828420754
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro1454Ser
CA020513
NM_001370405.1:c.4360C>T