Canonical Allele Identifier: PA2827020198
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616
ClinVar RCV Id: RCV004529305 RCV003512222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp1485Gly
CA394304815
NM_001318832.2:c.4454A>G