Canonical Allele Identifier: PA2826560646
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127808
ClinVar RCV Id: RCV000115719 RCV000122182 RCV000228299 RCV000589869 RCV000409407 RCV001358219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg71His
CA000123
NM_001276696.3:c.212G>A