Canonical Allele Identifier: PA2827020222
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 547827
ClinVar RCV Id: RCV000660349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val1491Asp
CA394304945
NM_001318832.2:c.4472T>A