Canonical Allele Identifier: PA645435969
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376591
ClinVar RCV Id: RCV000418557 RCV000418192 RCV000422952 RCV000423598 RCV000425968 RCV000428400 RCV000428433 RCV000431245 RCV000433190 RCV000435596 RCV000436841 RCV000435774 RCV000442043 RCV000441313 RCV000441497 RCV001048274 RCV004022211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Glu286Gln
CA16603013
NM_001126114.3:c.856G>C