ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826566705
Gene: TP53
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000165423
ClinVar Variation:
185918
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263690.1:p.Thr101Asn
CA000172
NM_001276761.3:c.302C>A