Canonical Allele Identifier: PA645436513
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1781Leu
CA10583347
NM_000548.5:c.5342C>T