Canonical Allele Identifier: PA2825436448
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.His763Tyr
CA038145
NM_001077183.3:c.2287C>T