ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA169757
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
142916
ClinVar RCV Id:
RCV000132389
RCV000679373
RCV000474969
RCV000663318
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Asn263Asp
CA000419
NM_001126113.3:c.787A>G