Canonical Allele Identifier: PA1139677632
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 940878
ClinVar RCV Id: RCV001210554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Gln38Pro
CA397847966
NM_001126114.3:c.113A>C