Canonical Allele Identifier: PA2828410250
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 952666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asp169Asn
CA394309180
NM_001370404.1:c.505G>A