Canonical Allele Identifier: PA2825606842
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480758
ClinVar RCV Id: RCV000565337
ClinVar Variation Id: 1462102
ClinVar RCV Id: RCV001954182 RCV003339855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Gly117Arg
CA397844409
NM_001126114.3:c.349G>C
CA397844412
NM_001126114.3:c.349G>A