ClinGen Allele Registry
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Canonical Allele Identifier:
PA196607
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
2.0887769626
Score
-1.1523521175
Score
0.300653906
Score
0.5376109281
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000166739
RCV000417885
RCV000420162
RCV000420721
RCV000424608
RCV000425235
RCV000426124
RCV000430982
RCV000432709
RCV000433509
RCV000434903
RCV000435516
RCV000441262
RCV000443587
RCV000444147
RCV001850353
ClinVar Variation:
187052
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Tyr163Asp
CA000239
NM_000546.6:c.487T>G