Canonical Allele Identifier: PA2826559882
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 234036
ClinVar RCV Id: RCV000223044 RCV000428477 RCV000421256 RCV000434302 RCV000423612 RCV000424282 RCV000441535 RCV000439114 RCV000426851 RCV000432300 RCV000433419 RCV000442741 RCV000560536 RCV001355898 RCV003137828 RCV003475037 RCV004020697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Asn200Asp
CA10580926
NM_001276695.3:c.598A>G