Canonical Allele Identifier: PA2826564070
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2969522
ClinVar RCV Id: RCV003821656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Asp48Asn
CA287488336
NM_001276699.3:c.142G>A