Canonical Allele Identifier: PA2826565850
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 232289
ClinVar RCV Id: RCV000221023 RCV000440110 RCV000441998 RCV000425285 RCV000432689 RCV000422868 RCV000432486 RCV000433813 RCV000633370 RCV002288875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ile216Asn
CA10580923
NM_001276760.3:c.647T>A