Canonical Allele Identifier: PA2826563829
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480740
ClinVar RCV Id: RCV000568856 RCV002509444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Gly166Arg
CA397835820
NM_001276698.3:c.496G>A
CA397835825
NM_001276698.3:c.496G>C