Canonical Allele Identifier: PA2825610788
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376578
ClinVar RCV Id: RCV000417879 RCV000418512 RCV000424746 RCV000425032 RCV000427153 RCV000433671 RCV000435743 RCV000435022 RCV000438269 RCV000442305 RCV000442449 RCV000688366 RCV000785473 RCV002379285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Cys110Phe
CA501203
NM_001126115.1:c.329G>T
CA645588597
NM_001126115.1:c.329_330delinsTT