ClinGen Allele Registry
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Canonical Allele Identifier:
PA916006306
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
234036
ClinVar RCV Id:
RCV000223044
RCV000428477
RCV000421256
RCV000434302
RCV000423612
RCV000424282
RCV000441535
RCV000439114
RCV000426851
RCV000432300
RCV000433419
RCV000442741
RCV000560536
RCV001355898
RCV003137828
RCV003475037
RCV004020697
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263628.1:p.Asn80Asp
CA10580926
NM_001276699.3:c.238A>G