Canonical Allele Identifier: PA2826564784
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406565
ClinVar RCV Id: RCV000459820 RCV001011072 RCV002289589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Met5Ile
CA16615713
NM_001276760.3:c.15G>A
CA397846847
NM_001276760.3:c.15G>T
CA397846851
NM_001276760.3:c.15G>C