Canonical Allele Identifier: PA2827003365
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp1046Val
CA019052
NM_001318827.2:c.3137A>T