Canonical Allele Identifier: PA2826561914
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376572
ClinVar RCV Id: RCV000421434 RCV000418563 RCV000424249 RCV000422732 RCV000424653 RCV000432087 RCV000429952 RCV000430137 RCV000429475 RCV000434070 RCV000439276 RCV000440822 RCV000441518 RCV000442369 RCV000445065 RCV000530055 RCV000567103 RCV000785243 RCV003401413 RCV004022205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Cys17Trp
CA16602998
NM_001276697.3:c.51C>G