Canonical Allele Identifier: PA2826565149
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 421437
ClinVar RCV Id: RCV000484833 RCV000662907 RCV001052030 RCV002289639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Met94Ile
CA16620633
NM_001276760.3:c.282G>A
CA397842844
NM_001276760.3:c.282G>C
CA397842845
NM_001276760.3:c.282G>T