Canonical Allele Identifier: PA2826567003
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 230256
ClinVar RCV Id: RCV000221478 RCV000424900 RCV000430089 RCV000436284 RCV000444740 RCV000445008 RCV000419469 RCV000419839 RCV000423524 RCV000426264 RCV000412758 RCV000418749 RCV000421204 RCV000440111 RCV000425998 RCV000431464 RCV000432551 RCV000429902 RCV000437380 RCV000441207 RCV000434647 RCV000441502 RCV000809571 RCV003332145 RCV002288851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.His154Tyr
CA10580936
NM_001276761.3:c.460C>T