Canonical Allele Identifier: PA2827010021
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 847781
ClinVar RCV Id: RCV001051397 RCV002339257 RCV003467763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1502Thr
CA394308162
NM_001318829.2:c.4504G>A