Canonical Allele Identifier: PA2825612861
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 575702
ClinVar Variation Id: 947223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.His46Gln
CA397841360
NM_001126116.1:c.138C>G
CA397841364
NM_001126116.1:c.138C>A