ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828414682
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
405960
ClinVar RCV Id:
RCV000459439
RCV001249140
RCV001022659
RCV004000680
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357333.1:p.Asp1468Asn
CA16614792
NM_001370404.1:c.4402G>A