ClinGen Allele Registry
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Canonical Allele Identifier:
PA195277
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.6952010418
Score
-1.345959549
Score
1.5787457153
Score
0.056557364
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000166212
RCV000419105
RCV000422986
RCV000423271
RCV000428907
RCV000433977
RCV000439592
RCV000439853
RCV000440211
RCV000785331
RCV001850338
RCV002288758
ClinVar Variation:
186594
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gln144Pro
CA000182
NM_000546.6:c.431A>C