ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA916006214
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376680
ClinVar RCV Id:
RCV000417511
RCV000418221
RCV000418859
RCV000423893
RCV000423239
RCV000425645
RCV000428451
RCV000431265
RCV000434193
RCV000435900
RCV000436639
RCV000438678
RCV000440924
RCV000441609
RCV001023195
RCV001071488
RCV002289543
RCV003476012
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263628.1:p.Tyr4His
CA16603094
NM_001276699.3:c.10T>C