Canonical Allele Identifier: PA2829975115
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406039
ClinVar RCV Id: RCV000457153 RCV000568724 RCV000765267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro672Leu
CA16615063
NM_021055.3:c.2015C>T