Canonical Allele Identifier: PA2826559792
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406592
ClinVar RCV Id: RCV000477098 RCV000564109 RCV003318578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro183Ser
CA16615720
NM_001276695.3:c.547C>T