ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA187495
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1081304109
Score
-0.65741455
Score
-2.752953014
Score
1.0684660672
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000163119
RCV000206777
RCV000478196
RCV000662787
RCV002465543
ClinVar Variation:
184014
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Thr170Met
CA000246
NM_000546.6:c.509C>T