Canonical Allele Identifier: PA2826567391
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 634680
ClinVar RCV Id: RCV000785271 RCV001869171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Asp220Tyr
CA397837654
NM_001276761.3:c.658G>T