Canonical Allele Identifier: PA2826559393
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376641
ClinVar RCV Id: RCV000418125 RCV000419693 RCV000420971 RCV000420838 RCV000425371 RCV000428371 RCV000426064 RCV000426471 RCV000431059 RCV000432886 RCV000431789 RCV000436762 RCV000437396 RCV000438632 RCV000441351 RCV000443299 RCV000443386 RCV000459465 RCV002338981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro112Ala
CA16603058
NM_001276695.3:c.334C>G