Canonical Allele Identifier: PA2826567162
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 635390
ClinVar Variation Id: 1493447
ClinVar RCV Id: RCV001984377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Glu185Asp
CA397839776
NM_001276761.3:c.555G>T
CA397839777
NM_001276761.3:c.555G>C