Canonical Allele Identifier: PA2826560701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182926
ClinVar RCV Id: RCV000161022 RCV001048454 RCV001527099 RCV000574455
ClinVar Variation Id: 1021578
ClinVar RCV Id: RCV001321369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys85Ser
CA000138
NM_001276696.3:c.253T>A
CA397844266
NM_001276696.3:c.254G>C