Canonical Allele Identifier: PA2826563022
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376017
ClinVar RCV Id: RCV000420735 RCV000421990 RCV000419648 RCV000420982 RCV000428561 RCV000430804 RCV000437348 RCV000432237 RCV000438619 RCV000438785 RCV000439921 RCV000437553 RCV000426247 RCV000445170 RCV000430991 RCV000436282 RCV000775880 RCV001237773 RCV002289516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Val14Ala
CA16602486
NM_001276698.3:c.41T>C