ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935597
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0304354211
Score
-2.995644397
Score
0.0575084054
Score
0.4879808743
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001201971
ClinVar Variation:
933702
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Leu188Val
CA397840905
NM_000546.6:c.562C>G