Canonical Allele Identifier: PA2825438713
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp1445Asn
CA16614792
NM_001077183.3:c.4333G>A