Canonical Allele Identifier: PA2828092822
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 664836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser956Asn
CA043671
NM_001363528.2:c.2867G>A