Canonical Allele Identifier: PA2826561129
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015039
ClinVar RCV Id: RCV001313852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gly160Arg
CA397840482
NM_001276696.3:c.478G>C
CA397840486
NM_001276696.3:c.478G>A