ClinGen Allele Registry
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Canonical Allele Identifier:
PA164835
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.2548147915
Score
0.8184130516
Score
-0.418943006
Score
0.848252481
Score
-0.9528867292
Score
0.00542649
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000129637
RCV000582737
RCV002510789
ClinVar Variation:
141224
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ile232Thr
CA000331
NM_000546.6:c.695T>C