ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826567122
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376672
ClinVar RCV Id:
RCV000418104
RCV000419558
RCV000418474
RCV000423283
RCV000424832
RCV000429825
RCV000429571
RCV000434860
RCV000436131
RCV000439819
RCV000440944
RCV002356519
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263690.1:p.Val177Glu
CA16603086
NM_001276761.3:c.530T>A