Canonical Allele Identifier: PA2825598628
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 822586
ClinVar RCV Id: RCV001018048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn29Asp
CA397848387
NM_001126112.3:c.85A>G