Canonical Allele Identifier: PA658679487
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482231
ClinVar RCV Id: RCV000561132 RCV000807881 RCV004024481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Val25Asp
CA397842047
NM_001126117.1:c.74T>A