ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA168692
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
142552
ClinVar RCV Id:
RCV000131746
RCV000195550
RCV001284721
RCV002267882
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Gly321Val
CA000030
NM_001126118.1:c.962G>T