ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826561261
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
480736
ClinVar RCV Id:
RCV000571914
RCV002289785
RCV001216966
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Val186Ile
CA397839539
NM_001276696.3:c.556G>A