ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935817
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.1650990428
Score
0.0028476183
Score
-3.777399954
Score
0.8980468978
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000786835
RCV001302589
RCV002292581
RCV002343642
ClinVar Variation:
635392
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly187Arg
CA397841073
NM_000546.6:c.559G>C