Canonical Allele Identifier: PA2825187594
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Asp1541Gly
CA394304815
NM_000548.5:c.4622A>G