Allele Registry

Canonical Allele Identifier: PA2826560750

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376624

ClinVar RCV Id: RCV000419339 RCV000422634 RCV000421516 RCV000424592 RCV000427056 RCV000430184 RCV000430063 RCV000432417 RCV000434424 RCV000432219 RCV000437720 RCV000439586 RCV000439834 RCV000440843 RCV000442346 RCV000442734 RCV000709407 RCV004022223

ClinVar Variation Id: 634773

ClinVar RCV Id: RCV000785513 RCV000795096 RCV003238212 RCV004027350

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Lys93Asn	CA16603044 NM_001276696.3:c.279G>C CA287488695 NM_001276696.3:c.279G>T