Canonical Allele Identifier: PA2826559932
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 265357
ClinVar RCV Id: RCV000255018 RCV000425368 RCV000428537 RCV000421477 RCV000431752 RCV000422531 RCV000432804 RCV000433958 RCV000436773 RCV000438479 RCV000443789 RCV000443845 RCV000420237 RCV000426521 RCV000442824 RCV000427619 RCV000437884 RCV002379095 RCV003509522 RCV003995742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Gly206Ala
CA10588670
NM_001276695.3:c.617G>C