Canonical Allele Identifier: PA2826565738
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376637
ClinVar RCV Id: RCV000427640 RCV000429581 RCV000436108 RCV000437044 RCV000442626 RCV000567507 RCV001851021 RCV002510885 RCV000418854 RCV000420011 RCV000426368 RCV000428926 RCV000438332 RCV000438482 RCV002289529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn200Ser
CA16603054
NM_001276760.3:c.599A>G
CA645588625
NM_001276760.3:c.599_600delinsGT