Canonical Allele Identifier: PA916006387
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 184882
ClinVar RCV Id: RCV000164218 RCV000785503 RCV001338713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asn88Ile
CA000378
NM_001276699.3:c.263A>T
CA645588553
NM_001276699.3:c.263_264delinsTA