ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563664
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127824
ClinVar RCV Id:
RCV000115739
RCV000122178
RCV000148912
RCV000200641
RCV000585912
RCV001357872
RCV000238755
RCV002477279
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Arg124Cys
CA000457
NM_001276698.3:c.370C>T