ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936236
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5867888992
Score
-1.186156104
Score
0.1935552996
Score
0.2514127475
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000492685
RCV000799619
RCV002289662
ClinVar Variation:
428863
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asp148Tyr
CA397842304
NM_000546.6:c.442G>T