ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825603490
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376626
ClinVar RCV Id:
RCV000417803
RCV000417874
RCV000423644
RCV000425237
RCV000426379
RCV000430828
RCV000428580
RCV000431096
RCV000433855
RCV000436180
RCV000434893
RCV000435981
RCV000440656
RCV000441816
RCV000442199
RCV000444903
RCV000468362
RCV000562533
RCV001253548
RCV004017609
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Lys132Glu
CA002647
NM_001126113.3:c.394A>G