ClinGen Allele Registry
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Canonical Allele Identifier:
PA151496
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
133262
ClinVar RCV:
RCV000115716
RCV000409540
RCV000679367
RCV001082818
RCV001796963
RCV003891612
ClinVar Variation:
127805
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Ala83Val
CA000083
NM_001126113.3:c.248C>T