ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935570
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.1554664523
Score
1.147751585
Score
-1.4349097445
Score
0.351111584
Score
-0.248880995
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000484792
RCV000551566
RCV001527084
RCV002350050
ClinVar Variation:
418517
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro190Leu
CA16620625
NM_000546.6:c.569C>T