ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825604244
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376609
ClinVar RCV Id:
RCV000419091
RCV000418067
RCV000419301
RCV000422109
RCV000422797
RCV000424599
RCV000424807
RCV000427824
RCV000429415
RCV000430449
RCV000433706
RCV000434154
RCV000433494
RCV000435925
RCV000434865
RCV000440508
RCV000440898
RCV000445154
RCV000444321
RCV000564826
RCV000695193
RCV001575036
RCV004022218
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.His179Asn
CA16603030
NM_001126113.3:c.535C>A