Canonical Allele Identifier: PA169514
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142828
ClinVar RCV Id: RCV000132259 RCV000785297 RCV003237742 RCV002288655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg205Leu
CA000015
NM_001126115.1:c.614G>T