ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579934259
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.0976428108
Score
-0.0864070605
Score
-2.140749274
Score
0.2230098589
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000457955
RCV000573281
RCV001724012
ClinVar Variation:
406577
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Lys292Arg
CA16615993
NM_000546.6:c.875A>G