Canonical Allele Identifier: PA2828094610
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1475Asn
CA276754962
NM_001363528.2:c.4423G>A