Canonical Allele Identifier: PA2826562012
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376635
ClinVar RCV Id: RCV000419057 RCV000424516 RCV000423937 RCV000425646 RCV000426810 RCV000433582 RCV000436323 RCV000433343 RCV000441162 RCV000441887 RCV000442808 RCV000633391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Leu35Pro
CA16603053
NM_001276697.3:c.104T>C