Canonical Allele Identifier: PA2828409932
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.His76Tyr
CA038111
NM_001370404.1:c.226C>T