Canonical Allele Identifier: PA2826559647
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376634
ClinVar RCV Id: RCV000422209 RCV000427064 RCV000434795 RCV000442619 RCV000443173 RCV000565549 RCV000785543 RCV000421586 RCV004022230 RCV000426499 RCV000431615 RCV000431831 RCV000436747 RCV000443531 RCV001376885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Leu155His
CA16603052
NM_001276695.3:c.464T>A