Canonical Allele Identifier: PA2826563632
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_001263627.1:p.Gly120Arg
CA397836876
NM_001276698.3:c.358G>C
CA397836877
NM_001276698.3:c.358G>A