Canonical Allele Identifier: PA2827020457
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497447
ClinVar RCV Id: RCV003213902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Met1559Val
CA394308148
NM_001318832.2:c.4675A>G