Canonical Allele Identifier: PA168659
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142536
ClinVar RCV Id: RCV000131726 RCV000475086 RCV000785479 RCV001310211 RCV001781474 RCV003467184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg205Cys
CA000010
NM_001126115.1:c.613C>T