Canonical Allele Identifier: PA2826561812
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497451
ClinVar RCV Id: RCV001996088
ClinVar Variation Id: 2832740
ClinVar RCV Id: RCV003622942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gln292His
CA287486501
NM_001276696.3:c.876G>T
CA397835662
NM_001276696.3:c.876G>C