ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579935878
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.2237701765
Score
1.5866390662
Score
1.2419360775
Score
0.135244427
Linked Data - NCBI & NCI
ClinVar Allele:
420659
ClinVar RCV:
RCV000492442
RCV000702915
RCV004023278
ClinVar Variation:
428866
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.His168Arg
CA287488569
NM_000546.6:c.503A>G