Canonical Allele Identifier: PA2827010183
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1560Gln
CA394311256
NM_001318829.2:c.4679C>A