Canonical Allele Identifier: PA2826567848
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 945439
ClinVar RCV Id: RCV001216083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg324Ser
CA397831840
NM_001276761.3:c.972G>T
CA397831841
NM_001276761.3:c.972G>C