Canonical Allele Identifier: PA2827016044
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn1399His
CA021298
NM_001318831.2:c.4195A>C