ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA645438167
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376666
ClinVar RCV Id:
RCV000418295
RCV000417666
RCV000422630
RCV000423200
RCV000425049
RCV000426486
RCV000428307
RCV000427158
RCV000429194
RCV000432449
RCV000433906
RCV000434887
RCV000436394
RCV000434566
RCV000439620
RCV000437835
RCV000439813
RCV000442101
RCV000442185
RCV000443332
RCV001041773
RCV004022243
RCV004022244
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Thr86Pro
CA16603081
NM_001126118.1:c.256A>C