Canonical Allele Identifier: PA2826566568
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406593
ClinVar RCV Id: RCV000477161 RCV000566683 RCV002289601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro41Ser
CA16615999
NM_001276761.3:c.121C>T