Canonical Allele Identifier: PA164099
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 135948
ClinVar RCV Id: RCV000123095 RCV000129275 RCV000410497 RCV001030740 RCV001192616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Asp10His
CA000057
NM_001126118.1:c.28G>C