Canonical Allele Identifier: PA2827015701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238055
ClinVar RCV Id: RCV000233971 RCV003165608 RCV003463660 RCV003998830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ile1301Val
CA10583336
NM_001318831.2:c.3901A>G