Canonical Allele Identifier: PA167038
Gene: TP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn131Tyr
CA000154
NM_001126112.3:c.391A>T