Canonical Allele Identifier: PA2828412000
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg680Trp
CA10579879
NM_001370404.1:c.2038C>T