Canonical Allele Identifier: PA645435692
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376665
ClinVar RCV Id: RCV000418366 RCV000419457 RCV000422775 RCV000420564 RCV000423557 RCV000425684 RCV000424609 RCV000426866 RCV000429686 RCV000432077 RCV000434790 RCV000434877 RCV000437125 RCV000435947 RCV000440449 RCV000441961 RCV000441702 RCV000441931 RCV000443160 RCV001045859 RCV002374627 RCV004022242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Ser241Ala
CA16603080
NM_001126114.3:c.721T>G