Canonical Allele Identifier: PA2825439243
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Thr1594Asn
CA394309184
NM_001077183.3:c.4781C>A