ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825610920
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376653
ClinVar RCV Id:
RCV000419533
RCV000420945
RCV000421561
RCV000420239
RCV000422393
RCV000430463
RCV000428988
RCV000429799
RCV000431805
RCV000434651
RCV000437240
RCV000439247
RCV000440059
RCV000445070
RCV000445103
RCV000690948
RCV000782360
RCV004022239
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119587.1:p.Arg117Met
CA16603070
NM_001126115.1:c.350G>T