Canonical Allele Identifier: PA2826564000
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376614
ClinVar RCV Id: RCV000420192 RCV000420894 RCV000419544 RCV000421458 RCV000422179 RCV000422815 RCV000426753 RCV000427057 RCV000428079 RCV000432133 RCV000430888 RCV000432878 RCV000433595 RCV000437420 RCV000439335 RCV000437710 RCV000438671 RCV000441851 RCV000441629 RCV000444677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.His34Asn
CA16603035
NM_001276699.3:c.100C>A