ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952310
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.330283579
Score
-0.213272426
Score
0.6632355333
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000486525
RCV000633374
RCV000774786
ClinVar Variation:
420974
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro295Leu
CA001416
NM_000546.6:c.884C>T