Canonical Allele Identifier: PA645435518
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 237943
ClinVar RCV Id: RCV000230713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro71Arg
CA10583684
NM_001126114.3:c.212C>G