Canonical Allele Identifier: PA167705
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142183
ClinVar RCV Id: RCV000131168 RCV000421075 RCV000418648 RCV000428270 RCV000419715 RCV000429365 RCV000435853 RCV000436923 RCV000438979 RCV000440030 RCV000421570 RCV000430428 RCV001214095 RCV004019744
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr104Asp
CA000344
NM_001126115.1:c.310T>G