Canonical Allele Identifier: PA2828414682
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asp1468Asn
CA16614792
NM_001370404.1:c.4402G>A