ClinGen Allele Registry
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Canonical Allele Identifier:
PA107174
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5698985347
Score
0.8046445443
Score
-0.725667358
Score
0.41108756
Score
1.553754553
Linked Data - NCBI & NCI
ClinVar Allele:
106675
ClinVar RCV:
RCV000087173
RCV000161036
RCV000460370
RCV000785556
RCV002288585
ClinVar Variation:
100815
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Met246Val
CA000374
NM_000546.6:c.736A>G