Canonical Allele Identifier: PA2826563699
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127825
ClinVar RCV Id: RCV000115740 RCV000148914 RCV000213061 RCV001357075 RCV001798340 RCV000620742 RCV003935102 RCV000760102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg131His
CA000468
NM_001276698.3:c.392G>A