Canonical Allele Identifier: PA2826560740
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216466
ClinVar RCV Id: RCV000200055 RCV000571787 RCV002271460 RCV002288816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Leu91Phe
CA339065
NM_001276696.3:c.271C>T