ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579953773
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.187896583
Score
0.4286859138
Score
-0.228925692
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000546598
RCV000563835
RCV002289723
ClinVar Variation:
458528
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro77Thr
CA003025
NM_000546.6:c.229C>A