ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2579954760
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.6784594728
Score
-0.0137607251
Score
-0.6230530441
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000463583
RCV000774798
RCV002289605
ClinVar Variation:
406608
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro47Thr
CA16615959
NM_000546.6:c.139C>A