Canonical Allele Identifier: PA2826560133
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376646
ClinVar RCV Id: RCV000417607 RCV000420265 RCV000422133 RCV000424797 RCV000426301 RCV000427682 RCV000428293 RCV000433513 RCV000433712 RCV000435517 RCV000437485 RCV000443564 RCV000444453 RCV000633329 RCV001017582 RCV002289531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro239His
CA16603063
NM_001276695.3:c.716C>A