Canonical Allele Identifier: PA658664695
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 481073
ClinVar RCV Id: RCV000567984 RCV003509564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ala80Pro
CA397844371
NM_001126118.1:c.238G>C