Canonical Allele Identifier: PA168060
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142320
ClinVar RCV Id: RCV000131382 RCV000168247 RCV000255239 RCV000576528 RCV001391195 RCV000989718 RCV001527471 RCV003462011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Arg49His
CA000259
NM_001126116.1:c.146G>A