Canonical Allele Identifier: PA2826565785
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186737
ClinVar RCV Id: RCV000166380 RCV002516500
ClinVar Variation Id: 406586
ClinVar RCV Id: RCV000470073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Met207Leu
CA000373
NM_001276760.3:c.619A>C
CA16615691
NM_001276760.3:c.619A>T