Canonical Allele Identifier: PA658692053
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ser67Arg
CA397844688
NM_001126118.1:c.201C>G
CA397844691
NM_001126118.1:c.201C>A
CA397844720
NM_001126118.1:c.199A>C