Canonical Allele Identifier: PA2826561565
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376674
ClinVar RCV Id: RCV000418736 RCV000419355 RCV000430114 RCV000428932 RCV000429450 RCV000435470 RCV000436116 RCV001255677 RCV001344689 RCV002429349 RCV000418237 RCV004022248 RCV000423526 RCV000440120 RCV000440773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Val235Phe
CA16603088
NM_001276696.3:c.703G>T