Canonical Allele Identifier: PA1139678496
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 956854
ClinVar RCV Id: RCV001229735 RCV002348773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro45His
CA397841407
NM_001126117.1:c.134C>A
CA645588943
NM_001126117.1:c.134_135delinsAT