Canonical Allele Identifier: PA2826562528
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376589
ClinVar RCV Id: RCV000417517 RCV000419849 RCV000420104 RCV000422679 RCV000424893 RCV000427537 RCV000425979 RCV000429708 RCV000430790 RCV000433406 RCV000435611 RCV000435784 RCV000438210 RCV000440361 RCV000440602 RCV000442214 RCV000443934 RCV000442965 RCV003463826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Asp122Ala
CA16603011
NM_001276697.3:c.365A>C