Canonical Allele Identifier: PA2825600084
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 575702
ClinVar Variation Id: 947223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.His178Gln
CA397841360
NM_001126112.3:c.534C>G
CA397841364
NM_001126112.3:c.534C>A