Canonical Allele Identifier: PA2826559696
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376684
ClinVar RCV Id: RCV000417461 RCV000419577 RCV000420753 RCV000422784 RCV000426051 RCV000424682 RCV000424892 RCV000430294 RCV000430575 RCV000432365 RCV000433474 RCV000435608 RCV000437987 RCV000441202 RCV000444368 RCV000444287 RCV000662621 RCV001024933 RCV001851022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr166Asn
CA16603098
NM_001276695.3:c.496T>A