ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA287657
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127806
ClinVar RCV Id:
RCV000115717
RCV000203717
RCV000235217
RCV000662410
RCV000781916
RCV000989729
RCV003905099
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119586.1:p.Val10Ile
CA000093
NM_001126114.3:c.28G>A