Canonical Allele Identifier: PA2825435834
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 509382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser592Asn
CA033474
NM_001077183.3:c.1775G>A