ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829972692
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
58835
ClinVar RCV:
RCV000042935
RCV002513627
ClinVar Variation:
49673
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Arg381Lys
CA013922
NM_021055.3:c.1142G>A