Canonical Allele Identifier: PA2825435540
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp501Asn
CA394326047
NM_001077183.3:c.1501G>A