Canonical Allele Identifier: PA2826567684
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071811
ClinVar RCV Id: RCV004016305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Lys281Thr
CA397835900
NM_001276761.3:c.842A>C