Canonical Allele Identifier: PA2828415427
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Met1671Val
CA021857
NM_001370404.1:c.5011A>G