Canonical Allele Identifier: PA2826567636
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485027
ClinVar RCV Id: RCV000568377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala268Gly
CA397836168
NM_001276761.3:c.803C>G