Canonical Allele Identifier: PA195712
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186737
ClinVar Variation Id: 406586
ClinVar RCV Id: RCV000470073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Met207Leu
CA000373
NM_001126118.1:c.619A>C
CA16615691
NM_001126118.1:c.619A>T