Canonical Allele Identifier: PA2826563647
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376586
ClinVar RCV Id: RCV000418705 RCV000421233 RCV000422096 RCV000424002 RCV000426180 RCV000426863 RCV000428837 RCV000428968 RCV000429505 RCV000431489 RCV000434267 RCV000437075 RCV000436424 RCV000439749 RCV000438896 RCV000442054 RCV000443405 RCV000443489 RCV000785452 RCV000824609 RCV002446642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Asp122Asn
CA001503
NM_001276698.3:c.364G>A