Canonical Allele Identifier: PA2825598456
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1485939
ClinVar RCV Id: RCV002001110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro4Ser
CA397849442
NM_001126112.3:c.10C>T