Canonical Allele Identifier: PA2826564859
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480745
ClinVar RCV Id: RCV000565744 RCV003621547 RCV002289791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Met27Ile
CA397846006
NM_001276760.3:c.81G>A
CA397846013
NM_001276760.3:c.81G>T
CA397846016
NM_001276760.3:c.81G>C