Canonical Allele Identifier: PA645432032
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro541Arg
CA031797
NM_000548.5:c.1622C>G