ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825600550
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
363551
ClinVar RCV:
RCV000418104
RCV000418474
RCV000419558
RCV000423283
RCV000424832
RCV000429571
RCV000429825
RCV000434860
RCV000436131
RCV000439819
RCV000440944
RCV002356519
ClinVar Variation:
376672
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119584.1:p.Val216Glu
CA16603086
NM_001126112.3:c.647T>A