Canonical Allele Identifier: PA2828413654
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468031
ClinVar RCV Id: RCV000530877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro1171Ala
CA394291882
NM_001370404.1:c.3511C>G