Canonical Allele Identifier: PA2825439292
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1608Gln
CA394311256
NM_001077183.3:c.4823C>A