Canonical Allele Identifier: PA2827005468
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp1631Val
CA10583344
NM_001318827.2:c.4892A>T