ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA107353
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.4914446304
Score
1.4748505636
Score
-1.1614749527
Score
-0.963599056
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000167874
RCV001024656
RCV002288770
ClinVar Variation:
188060
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val197Met
CA000285
NM_000546.6:c.589G>A