Canonical Allele Identifier: PA2827020992
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1695His
CA054581
NM_001318832.2:c.5084G>A