Canonical Allele Identifier: PA2828415715
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro1737Leu
CA10583347
NM_001370404.1:c.5210C>T