ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA168693
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.7473002825
Score
-0.7977132769
Score
-0.6082654199
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000131746
RCV000195550
RCV001284721
RCV002267882
ClinVar Variation:
142552
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly360Val
CA000030
NM_000546.6:c.1079G>T