Canonical Allele Identifier: PA2826559363
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186594
ClinVar RCV Id: RCV000166212 RCV000422986 RCV000433977 RCV000440211 RCV000423271 RCV000439592 RCV000419105 RCV000428907 RCV000439853 RCV000785331 RCV002288758 RCV001850338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Gln105Pro
CA000182
NM_001276695.3:c.314A>C