ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579954774
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.2155555051
Score
-0.634663357
Score
-0.2051952557
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002305383
ClinVar Variation:
1721838
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro47Ala
CA397846769
NM_000546.6:c.139C>G