ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952687
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.8989732742
Score
1.1020806832
Score
-0.024872345
Score
-1.0536511614
Score
-0.653685699
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000459389
RCV002272239
RCV004022605
ClinVar Variation:
406590
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Glu258Gly
CA16615703
NM_000546.6:c.773A>G