ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579951526
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.7820948465
Score
-0.4418711578
Score
-0.5550974356
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000479182
RCV001037256
RCV002289636
RCV002289637
ClinVar Variation:
421319
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gln331Arg
CA16620611
NM_000546.6:c.992A>G