Canonical Allele Identifier: PA2827020676
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1619Gln
CA394311256
NM_001318832.2:c.4856C>A