Canonical Allele Identifier: PA2826567442
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376597
ClinVar RCV Id: RCV000422121 RCV000422786 RCV000424190 RCV000432351 RCV000434574 RCV000433925 RCV000440467 RCV000441020 RCV000443933 RCV001805037 RCV002508212 RCV002524696 RCV003470375 RCV004022213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Phe231Cys
CA16603019
NM_001276761.3:c.692T>G