Canonical Allele Identifier: PA2826559651
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376618
ClinVar RCV Id: RCV000417492 RCV000419606 RCV000420311 RCV000422932 RCV000424894 RCV000427719 RCV000425779 RCV000430554 RCV000432578 RCV000435160 RCV000433212 RCV000437965 RCV000440578 RCV000440765 RCV000442006 RCV000444669 RCV000692717 RCV000785514 RCV001024599 RCV002289528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ile156Asn
CA16603038
NM_001276695.3:c.467T>A