Canonical Allele Identifier: PA319360
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His763Tyr
CA038145
NM_000548.5:c.2287C>T