ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2579954382
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.1352574312
Score
0.3711905532
Score
0.1617227112
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000562780
RCV000822098
RCV002289833
ClinVar Variation:
485040
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asp41Asn
CA397847025
NM_000546.6:c.121G>A