Canonical Allele Identifier: PA132779
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 43588
ClinVar RCV Id: RCV000036530 RCV000131567 RCV000172826 RCV000590436 RCV000991144 RCV001355028 RCV002225273 RCV002496568 RCV003149630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro47Ser
CA000053
NM_001126114.3:c.139C>T