Canonical Allele Identifier: PA2827020955
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1687Pro
CA022224
NM_001318832.2:c.5060G>C