Canonical Allele Identifier: PA2825438577
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp1411Asn
CA394302242
NM_001077183.3:c.4231G>A