ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579950971
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.7681141315
Score
-2.1969541981
Score
0.8805870606
Linked Data - NCBI & NCI
ClinVar Allele:
479232
ClinVar RCV:
RCV000569933
RCV001035792
ClinVar Variation:
485050
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr387Arg
CA287485465
NM_000546.6:c.1160C>G