Canonical Allele Identifier: PA2825606191
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087249
ClinVar RCV Id: RCV003017803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Met44Leu
CA397846872
NM_001126114.3:c.130A>T
CA397846886
NM_001126114.3:c.130A>C