Canonical Allele Identifier: PA2825576791
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1506Trp
CA276754888
NM_001114382.3:c.4516C>T