Canonical Allele Identifier: PA916006712
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_001263690.1:p.Leu91Phe
CA339065
NM_001276761.3:c.271C>T