Canonical Allele Identifier: PA2828093724
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asn1227Ser
CA394293642
NM_001363528.2:c.3680A>G