Canonical Allele Identifier: PA645436162
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.His47Arg
CA16603027
NM_001126117.1:c.140A>G