Canonical Allele Identifier: PA167708
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
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Tyr197Asp
CA000344
NM_001126118.1:c.589T>G