Canonical Allele Identifier: PA916023017
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405981
ClinVar RCV Id: RCV000461553 RCV001019998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala866Gly
CA16614990
NM_001318831.2:c.2597C>G