Canonical Allele Identifier: PA645436172
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376608
ClinVar RCV Id: RCV000418129 RCV000420124 RCV000418835 RCV000421837 RCV000426806 RCV000427330 RCV000427517 RCV000429543 RCV000427941 RCV000433134 RCV000432531 RCV000432746 RCV000435347 RCV000438217 RCV000438631 RCV000439318 RCV000439930 RCV000444683 RCV000443637 RCV000705316 RCV002348143 RCV003476009 RCV004022217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His47Leu
CA16603029
NM_001126117.1:c.140A>T