Canonical Allele Identifier: PA2827010463
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1637Glu
CA394314782
NM_001318829.2:c.4909C>G