Canonical Allele Identifier: PA2826561000
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12374
ClinVar RCV Id: RCV000013173 RCV000131301 RCV000204931 RCV000239398 RCV000213054 RCV000421746 RCV000428918 RCV000785352 RCV001255668 RCV001270268 RCV001270269 RCV001527463 RCV002476956 RCV003162247 RCV003466854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg136His
CA000251
NM_001276696.3:c.407G>A