Canonical Allele Identifier: PA2826567296
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376604
ClinVar RCV Id: RCV000418277 RCV000420527 RCV000419444 RCV000424643 RCV000425790 RCV000426804 RCV000429713 RCV000432081 RCV000430767 RCV000431462 RCV000436041 RCV000437043 RCV000439119 RCV000441708 RCV000444043 RCV000444128 RCV000633351 RCV001026295 RCV004022215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly206Arg
CA16603025
NM_001276761.3:c.616G>C