Canonical Allele Identifier: PA915980141
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826165
ClinVar RCV Id: RCV001024853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg70Pro
CA397840404
NM_001126117.1:c.209G>C
CA645588790
NM_001126117.1:c.209_210delinsCG