Canonical Allele Identifier: PA2828421634
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1687Val
CA10583344
NM_001370405.1:c.5060A>T