Canonical Allele Identifier: PA2825612387
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376564
ClinVar RCV Id: RCV000425931 RCV000423924 RCV000424802 RCV000422816 RCV000430241 RCV000434169 RCV000431589 RCV000434797 RCV000445034 RCV000440499 RCV000442353 RCV000492201 RCV000444942 RCV000467641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Cys9Trp
CA16602990
NM_001126116.1:c.27C>G