ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827002061
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
467917
ClinVar RCV Id:
RCV000554874
RCV000563982
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305756.1:p.Ala638Leu
CA658658369
NM_001318827.2:c.1912_1913delinsTT