ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579934284
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376646
ClinVar RCV Id:
RCV000417607
RCV000420265
RCV000422133
RCV000424797
RCV000426301
RCV000427682
RCV000428293
RCV000433513
RCV000433712
RCV000435517
RCV000437485
RCV000443564
RCV000444453
RCV000633329
RCV001017582
RCV002289531
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro278His
CA16603063
NM_000546.6:c.833C>A