ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA107137
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-1.0974527257
Score
0.9553557213
Score
1.4599184919
Score
0.165258322
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003484944
ClinVar Variation:
2687699
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Met133Arg
CA397842848
NM_000546.6:c.398T>G