ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA169189
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.2068883925
Score
0.0679539652
Score
-0.7142126214
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000132069
RCV001050775
RCV002288653
ClinVar Variation:
142702
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr304Ala
CA000493
NM_000546.6:c.910A>G