Canonical Allele Identifier: PA2826561899
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376669
ClinVar RCV Id: RCV000421130 RCV000419351 RCV000420346 RCV000425882 RCV000425654 RCV000430605 RCV000430481 RCV000431387 RCV000437016 RCV000435883 RCV000437139 RCV000441782 RCV000442089 RCV000443047 RCV000443122 RCV000574130 RCV000582350 RCV002524700 RCV004022245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Val14Glu
CA16603083
NM_001276697.3:c.41T>A