Canonical Allele Identifier: PA916006349
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376599
ClinVar RCV Id: RCV000419449 RCV000418385 RCV000422508 RCV000427774 RCV000430162 RCV000427875 RCV000429067 RCV000438569 RCV000436692 RCV000437805 RCV000437360 RCV000439724 RCV000443459 RCV000538079 RCV001270273 RCV001567979 RCV002379286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Gly85Cys
CA16603021
NM_001276699.3:c.253G>T