Canonical Allele Identifier: PA645438182
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376628
ClinVar RCV Id: RCV000419400 RCV000421029 RCV000419226 RCV000422568 RCV000427319 RCV000427528 RCV000429238 RCV000432840 RCV000432114 RCV000434062 RCV000436873 RCV000438684 RCV000440130 RCV000439934 RCV000442713 RCV000442639 RCV001205860 RCV003463827 RCV004022226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Lys93Gln
CA16603047
NM_001126118.1:c.277A>C