Canonical Allele Identifier: PA2825598895
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528264
ClinVar RCV Id: RCV000633377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Pro67Gln
CA397845972
NM_001126112.3:c.200C>A