ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935321
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.5798639393
Score
-0.05982054
Score
0.241763445
Score
-0.598726133
Score
1.3645443402
Score
0.8404218058
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000633350
RCV001175697
RCV002289924
ClinVar Variation:
528249
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val218Gly
CA397839930
NM_000546.6:c.653T>G