Canonical Allele Identifier: PA2826567004
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376612
ClinVar RCV Id: RCV000417520 RCV000418213 RCV000422374 RCV000422912 RCV000423516 RCV000424851 RCV000429577 RCV000427668 RCV000428197 RCV000428877 RCV000434205 RCV000433585 RCV000434933 RCV000435420 RCV000435566 RCV000440128 RCV000439568 RCV000442541 RCV000444985 RCV000445292 RCV000991151 RCV001525967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.His154Pro
CA16603033
NM_001276761.3:c.461A>C