Canonical Allele Identifier: PA2826560722
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182928
ClinVar RCV Id: RCV000161024 RCV000633384 RCV000606528 RCV000785332 RCV003162681 RCV004019945 RCV003474836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ser88Phe
CA000148
NM_001276696.3:c.263C>T
CA645589213
NM_001276696.3:c.263_264delinsTT