ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579955141
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.3077991847
Score
-0.0618306084
Score
-0.140919575
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000220312
RCV000550564
RCV001575870
RCV002288887
ClinVar Variation:
233248
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gln5Arg
CA003990
NM_000546.6:c.14A>G