Canonical Allele Identifier: PA2826563418
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376602
ClinVar RCV Id: RCV000419267 RCV000420351 RCV000418001 RCV000424520 RCV000425133 RCV000425485 RCV000430145 RCV000431028 RCV000432729 RCV000435229 RCV000437599 RCV000438254 RCV000443153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Gly85Arg
CA16603024
NM_001276698.3:c.253G>C