ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA215796
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.148697571
Score
-0.6033896705
Score
-0.9069770227
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000034640
RCV000161016
RCV000213044
RCV000226569
RCV001030742
RCV001124310
RCV003924896
ClinVar Variation:
41723
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu11Gln
CA000106
NM_000546.6:c.31G>C