Canonical Allele Identifier: PA168938
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142624
ClinVar RCV Id: RCV000131943 RCV000168292 RCV000236276 RCV003474780 RCV004544301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Arg49Cys
CA000257
NM_001126115.1:c.145C>T
CA645588898
NM_001126115.1:c.145_150delinsTGCTGT