ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826561535
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376596
ClinVar RCV Id:
RCV000418371
RCV000417655
RCV000417883
RCV000425994
RCV000427865
RCV000430718
RCV000436003
RCV000436185
RCV000438999
RCV000785257
RCV001362325
RCV002418243
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263625.1:p.Phe231Ile
CA16603018
NM_001276696.3:c.691T>A