ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA168220
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
142386
ClinVar RCV Id:
RCV000131474
RCV000553568
RCV000986048
RCV001192621
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119586.1:p.Val73Met
CA000075
NM_001126114.3:c.217G>A