Canonical Allele Identifier: PA658679405
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458568
ClinVar RCV Id: RCV000547189 RCV000566142 RCV002267618 RCV003459203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Gly279Arg
CA397836876
NM_001126114.3:c.835G>C
CA397836877
NM_001126114.3:c.835G>A