ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579953856
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.4403962281
Score
-0.1583438715
Score
0.2133627833
Linked Data - NCBI & NCI
ClinVar Allele:
531847
ClinVar RCV:
RCV000633366
RCV001014310
RCV002289927
ClinVar Variation:
528260
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Ala69Val
CA287489112
NM_000546.6:c.206C>T