Canonical Allele Identifier: PA2826565736
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 385614
ClinVar RCV Id: RCV000431317 RCV000492173 RCV000529909 RCV003463830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn200Lys
CA16607851
NM_001276760.3:c.600C>G
CA397839156
NM_001276760.3:c.600C>A