Canonical Allele Identifier: PA2825616691
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 490170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Glu29Gln
CA397845956
NM_001126118.1:c.85G>C