ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827004507
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000458532
RCV000500804
RCV001022474
RCV004000678
ClinVar Variation:
405956
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001305756.1:p.Ala1376Thr
CA16615031
NM_001318827.2:c.4126G>A