Canonical Allele Identifier: PA2826563058
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 421546
ClinVar RCV Id: RCV000485632 RCV003509545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.His19Asn
CA16620628
NM_001276698.3:c.55C>A