Canonical Allele Identifier: PA2829978619
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405981
ClinVar RCV Id: RCV000461553 RCV001019998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala1067Gly
CA16614990
NM_021055.3:c.3200C>G