Canonical Allele Identifier: PA2827007512
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro616Leu
CA394274421
NM_001318829.2:c.1847C>T