ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951975
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.3496679614
Score
0.4738034628
Score
0.0507774956
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000473016
RCV001805064
RCV002289599
ClinVar Variation:
406589
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asn311Ser
CA16615690
NM_000546.6:c.932A>G