Canonical Allele Identifier: PA2825611387
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376585
ClinVar RCV Id: RCV000419187 RCV000419880 RCV000421597 RCV000422382 RCV000422971 RCV000424398 RCV000427237 RCV000429763 RCV000431847 RCV000430133 RCV000432647 RCV000437480 RCV000438115 RCV000436876 RCV000440017 RCV000442319 RCV000442636 RCV000443331 RCV000792342 RCV004022209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Asp149Tyr
CA16603009
NM_001126115.1:c.445G>T