Canonical Allele Identifier: PA645436231
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 231165
ClinVar RCV Id: RCV000216410 RCV000418400 RCV000423798 RCV000427483 RCV000431695 RCV000443813 RCV000443927 RCV000419494 RCV000425092 RCV000429772 RCV000433800 RCV000435372 RCV000436292 RCV000426017 RCV000434064 RCV000440531 RCV000440866 RCV003114386 RCV004020663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg64Pro
CA10580934
NM_001126117.1:c.191G>C