Canonical Allele Identifier: PA2826561947
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509915
ClinVar RCV Id: RCV002011381
ClinVar Variation Id: 1521256
ClinVar RCV Id: RCV002031179 RCV002346322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Glu21Asp
CA397841280
NM_001276697.3:c.63G>T
CA397841283
NM_001276697.3:c.63G>C