ClinGen Allele Registry
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Canonical Allele Identifier:
PA162550
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0364105843
Score
-0.6449191394
Score
-0.0191940317
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000115715
RCV000122181
RCV000586104
RCV000662515
RCV001086750
RCV003492489
RCV003952551
ClinVar Variation:
127804
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro58Arg
CA000061
NM_000546.6:c.173C>G