Canonical Allele Identifier: PA2826562972
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376680
ClinVar RCV Id: RCV000417511 RCV000418221 RCV000418859 RCV000423893 RCV000423239 RCV000425645 RCV000428451 RCV000431265 RCV000434193 RCV000435900 RCV000436639 RCV000438678 RCV000440924 RCV000441609 RCV001023195 RCV001071488 RCV002289543 RCV003476012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Tyr4His
CA16603094
NM_001276698.3:c.10T>C