Canonical Allele Identifier: PA645432310
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg680Trp
CA10579879
NM_000548.5:c.2038C>T