Canonical Allele Identifier: PA2828409779
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 385045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro28His
CA16607134
NM_001370404.1:c.83C>A