Canonical Allele Identifier: PA2825183709
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro903Thr
CA394279461
NM_000548.5:c.2707C>A