Canonical Allele Identifier: PA2827000905
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Tyr312Cys
CA16614703
NM_001318827.2:c.935A>G