Canonical Allele Identifier: PA2826564507
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406585
ClinVar RCV Id: RCV000477030 RCV002374764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Gln158His
CA16615689
NM_001276699.3:c.474G>T
CA397835964
NM_001276699.3:c.474G>C