Canonical Allele Identifier: PA916023748
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_001305761.1:p.Pro683Leu
CA16615063
NM_001318832.2:c.2048C>T