Canonical Allele Identifier: PA2825577081
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318332
ClinVar RCV Id: RCV000330059 RCV000415620 RCV002338901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1589Asn
CA10637331
NM_001114382.3:c.4765G>A