ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826567523
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
363467
ClinVar RCV:
RCV000418744
RCV000419869
RCV000420094
RCV000421295
RCV000422034
RCV000423682
RCV000427301
RCV000427507
RCV000428355
RCV000429459
RCV000429671
RCV000434610
RCV000436837
RCV000437082
RCV000438193
RCV000439019
RCV000439212
RCV000443566
RCV001292542
RCV001306199
RCV002446644
RCV004022210
ClinVar Variation:
376588
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263690.1:p.Asp242His
CA16603010
NM_001276761.3:c.724G>C