Canonical Allele Identifier: PA891858122
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 575702
ClinVar RCV Id: RCV000698003 RCV001023959 RCV002307599
ClinVar Variation Id: 947223
ClinVar RCV Id: RCV001218247 RCV002348728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His46Gln
CA397841360
NM_001126117.1:c.138C>G
CA397841364
NM_001126117.1:c.138C>A