Canonical Allele Identifier: PA2826565198
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376565
ClinVar RCV Id: RCV000419723 RCV000420817 RCV000418678 RCV000423623 RCV000425407 RCV000432161 RCV000430017 RCV000437414 RCV000431037 RCV000436190 RCV000440220 RCV000441312 RCV001861481 RCV002328907
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Cys102Arg
CA16602991
NM_001276760.3:c.304T>C