Canonical Allele Identifier: PA287798
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127820
ClinVar RCV Id: RCV000115732 RCV000200601 RCV000438314 RCV000425220 RCV000425854 RCV000432406 RCV000433924 RCV000435287 RCV000445147 RCV000420460 RCV000430670 RCV000444325 RCV000444475 RCV000492245 RCV000420651 RCV000422171 RCV000435258 RCV000785536 RCV001808343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Tyr102Cys
CA000337
NM_001126117.1:c.305A>G