Canonical Allele Identifier: PA2825439715
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1714Leu
CA10583347
NM_001077183.3:c.5141C>T