Canonical Allele Identifier: PA2826562958
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161518
ClinVar RCV Id: RCV000149053 RCV000161027 RCV000214033 RCV000473543 RCV000761073 RCV000785328 RCV003474797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Ala2Thr
CA000234
NM_001276698.3:c.4G>A
CA645589015
NM_001276698.3:c.4_6delinsACT