Canonical Allele Identifier: PA2826564387
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376593
ClinVar RCV Id: RCV000419358 RCV000421888 RCV000421331 RCV000423414 RCV000424971 RCV000427672 RCV000430190 RCV000431576 RCV000433092 RCV000434375 RCV000439537 RCV000437905 RCV000443500 RCV000443287 RCV000444095 RCV004022212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Glu127Ala
CA16603015
NM_001276699.3:c.380A>C