Canonical Allele Identifier: PA2826564777
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 864154
ClinVar RCV Id: RCV001071270
ClinVar Variation Id: 1692471
ClinVar RCV Id: RCV002257219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Leu4Phe
CA003217
NM_001276760.3:c.12G>C
CA397846888
NM_001276760.3:c.12G>T