Canonical Allele Identifier: PA658680700
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His600Tyr
CA033559
NM_000548.5:c.1798C>T