Canonical Allele Identifier: PA2825436034
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp647Asn
CA016233
NM_001077183.3:c.1939G>A