Canonical Allele Identifier: PA2826561900
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376016
ClinVar RCV Id: RCV000418455 RCV000424145 RCV000419153 RCV000421182 RCV000429875 RCV000430527 RCV000426044 RCV000429147 RCV000432060 RCV000421399 RCV000441241 RCV000442290 RCV000432754 RCV000437220 RCV000441421 RCV000445056 RCV000807434 RCV003463825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Val14Gly
CA16602485
NM_001276697.3:c.41T>G