Canonical Allele Identifier: PA2826561902
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233951
ClinVar RCV Id: RCV000214341 RCV000223396 RCV000418173 RCV000418768 RCV000429546 RCV000435180 RCV000440133 RCV000418817 RCV000429913 RCV000423542 RCV000423333 RCV000424469 RCV000433605 RCV000434638 RCV000439338 RCV000435365 RCV000441217 RCV000477355 RCV000785308 RCV001255635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Val14Met
CA10577579
NM_001276697.3:c.40G>A