Canonical Allele Identifier: PA2825613454
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376693
ClinVar RCV Id: RCV000423298 RCV000428749 RCV000429935 RCV000437595 RCV000440629 RCV000444464 RCV000785279 RCV001201781 RCV001559774 RCV002365462 RCV000419208 RCV000420300 RCV000425130 RCV000430980 RCV000438183 RCV004022256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Tyr104Cys
CA16603106
NM_001126116.1:c.311A>G