ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935363
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.171882164
Score
-2.684737742
Score
0.3887451107
Score
-2.683768445
Score
-2.608555715
Score
0.1428373385
Score
-0.4475480775
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000571914
RCV001216966
RCV002289785
ClinVar Variation:
480736
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val225Ile
CA397839539
NM_000546.6:c.673G>A