Canonical Allele Identifier: PA2826565779
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376603
ClinVar RCV Id: RCV000418643 RCV000421020 RCV000421739 RCV000424123 RCV000426568 RCV000428216 RCV000429303 RCV000430431 RCV000434145 RCV000434833 RCV000435854 RCV000437258 RCV000439974 RCV000438982 RCV000443716 RCV000444483 RCV000558455 RCV001026313 RCV001548147 RCV002289525 RCV003476008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly206Val
CA001743
NM_001276760.3:c.617G>T
CA645588573
NM_001276760.3:c.617_618delinsTT