Canonical Allele Identifier: PA2826565836
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 837688
ClinVar RCV Id: RCV001039079 RCV003307815 RCV004031088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr214Ile
CA397838857
NM_001276760.3:c.641C>T