ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579935391
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.54404509
Score
0.2768609594
Score
-1.908157655
Score
-2.515216783
Score
0.6707200906
Score
0.0827642323
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000709405
RCV002289988
RCV002289989
ClinVar Variation:
584922
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asp208Gly
CA397840196
NM_000546.6:c.623A>G