Canonical Allele Identifier: PA645432312
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg680Gln
CA035970
NM_000548.5:c.2039G>A