ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579934320
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376677
ClinVar RCV Id:
RCV000420150
RCV000421817
RCV000426067
RCV000427353
RCV000426772
RCV000432482
RCV000433292
RCV000437438
RCV000438006
RCV000443517
RCV000444136
RCV001056029
RCV002429350
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val274Ala
CA16603091
NM_000546.6:c.821T>C