Canonical Allele Identifier: PA2825614032
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376676
ClinVar RCV Id: RCV000419865 RCV000421122 RCV000420544 RCV000426446 RCV000431168 RCV000431803 RCV000430539 RCV000437117 RCV000439046 RCV000441279 RCV000492506 RCV001255678 RCV004022249 RCV000438367 RCV000692432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Val142Gly
CA16603090
NM_001126116.1:c.425T>G