ClinGen Allele Registry
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Canonical Allele Identifier:
PA916006413
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
141881
ClinVar RCV Id:
RCV000130578
RCV000425504
RCV000432429
RCV000434278
RCV000440994
RCV000431276
RCV000432948
RCV000435888
RCV000443796
RCV000433563
RCV000435249
RCV000444809
RCV000417537
RCV000418238
RCV000423307
RCV000424980
RCV000426167
RCV002514731
RCV003237740
RCV003460931
RCV004019741
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263628.1:p.Arg90Trp
CA000389
NM_001276699.3:c.268A>T