Canonical Allele Identifier: PA2825615980
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
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Asp149Ala
CA16603011
NM_001126117.1:c.446A>C