Canonical Allele Identifier: PA2828095335
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1668Val
CA10583344
NM_001363528.2:c.5003A>T