Canonical Allele Identifier: PA2828411989
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169263
ClinVar RCV Id: RCV003082988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro677Ser
CA394274535
NM_001370404.1:c.2029C>T