Canonical Allele Identifier: PA645438167
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376666
ClinVar RCV Id: RCV000418295 RCV000417666 RCV000422630 RCV000423200 RCV000425049 RCV000426486 RCV000428307 RCV000427158 RCV000429194 RCV000432449 RCV000433906 RCV000434887 RCV000436394 RCV000434566 RCV000439620 RCV000437835 RCV000439813 RCV000442101 RCV000442185 RCV000443332 RCV001041773 RCV004022243 RCV004022244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Thr86Pro
CA16603081
NM_001126118.1:c.256A>C