Canonical Allele Identifier: PA2826565700
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127821
ClinVar RCV Id: RCV000115733 RCV000122177 RCV000148915 RCV000590586 RCV000663295 RCV000989714 RCV000991139 RCV001798339 RCV003952552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Asn196Ser
CA000343
NM_001276760.3:c.587A>G