Canonical Allele Identifier: PA2826559838
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376692
ClinVar RCV Id: RCV000417830 RCV000418444 RCV000423653 RCV000428072 RCV000426109 RCV000426512 RCV000426723 RCV000433276 RCV000434769 RCV000436114 RCV000436336 RCV000439167 RCV000444101 RCV000444893 RCV000809457 RCV001025925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr195Asn
CA16603105
NM_001276695.3:c.583T>A