Canonical Allele Identifier: PA2826567369
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376621
ClinVar RCV Id: RCV000418615 RCV000425759 RCV000428426 RCV000436027 RCV000435616 RCV000436676 RCV000444896 RCV000785451 RCV001301950 RCV002392946 RCV004022222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ile216Phe
CA16603041
NM_001276761.3:c.646A>T