Canonical Allele Identifier: PA645436166
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376610
ClinVar RCV Id: RCV000420116 RCV000419821 RCV000421694 RCV000423899 RCV000426383 RCV000424030 RCV000425288 RCV000430612 RCV000430072 RCV000431709 RCV000431956 RCV000436443 RCV000437679 RCV000436622 RCV000440707 RCV000441771 RCV000443866 RCV000444860 RCV000444992 RCV001851020 RCV002348144 RCV003470376 RCV002465649 RCV003335320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His47Asp
CA16603031
NM_001126117.1:c.139C>G