Canonical Allele Identifier: PA915978739
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 822586
ClinVar RCV Id: RCV001018048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Asn29Asp
CA397848387
NM_001126114.3:c.85A>G