Canonical Allele Identifier: PA645435947
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376588
ClinVar RCV Id: RCV000420094 RCV000418744 RCV000421295 RCV000419869 RCV000422034 RCV000423682 RCV000428355 RCV000427301 RCV000429459 RCV000427507 RCV000429671 RCV000434610 RCV000437082 RCV000436837 RCV000439019 RCV000438193 RCV000439212 RCV000443566 RCV001292542 RCV001306199 RCV002446644 RCV004022210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Asp281His
CA16603010
NM_001126114.3:c.841G>C