ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826564145
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000419021
RCV000419523
RCV000419702
RCV000421037
RCV000423767
RCV000424584
RCV000426310
RCV000427847
RCV000429130
RCV000429300
RCV000432093
RCV000434035
RCV000434427
RCV000437403
RCV000438068
RCV000438679
RCV000438838
RCV000439357
RCV000443812
RCV000570507
RCV001313857
RCV001575028
RCV004022254
ClinVar Variation:
376688
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263628.1:p.Tyr61Asn
CA16603101
NM_001276699.3:c.181T>A