Canonical Allele Identifier: PA2827015032
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238042
ClinVar RCV Id: RCV000227467 RCV003165607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ile1113Asn
CA10583331
NM_001318831.2:c.3338T>A