Canonical Allele Identifier: PA2825434545
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp162Asn
CA394309028
NM_001077183.3:c.484G>A