Canonical Allele Identifier: PA2825600889
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376637
ClinVar RCV Id: RCV000427640 RCV000429581 RCV000436108 RCV000437044 RCV000442626 RCV000567507 RCV001851021 RCV002510885 RCV000418854 RCV000420011 RCV000426368 RCV000428926 RCV000438332 RCV000438482 RCV002289529
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn239Ser
CA16603054
NM_001126112.3:c.716A>G
CA645588625
NM_001126112.3:c.716_717delinsGT