Canonical Allele Identifier: PA2826566354
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485038
ClinVar Variation Id: 657014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.His329Gln
CA397830872
NM_001276760.3:c.987C>G
CA397830875
NM_001276760.3:c.987C>A