Canonical Allele Identifier: PA168102
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142332
ClinVar RCV Id: RCV000131400 RCV000549010 RCV000760105 RCV001527095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Ser303Gly
CA000491
NM_001126112.3:c.907A>G