Canonical Allele Identifier: PA2827021125
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1725Leu
CA10583347
NM_001318832.2:c.5174C>T