ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935413
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376685
ClinVar RCV Id:
RCV000419308
RCV000420368
RCV000421826
RCV000422887
RCV000424493
RCV000427755
RCV000426781
RCV000431739
RCV000431958
RCV000432726
RCV000437451
RCV000437587
RCV000439923
RCV000440094
RCV000443622
RCV000443753
RCV000819983
RCV000775886
RCV004022252
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Tyr205His
CA16603099
NM_000546.6:c.613T>C