ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826559294
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376628
ClinVar RCV Id:
RCV000419400
RCV000421029
RCV000419226
RCV000422568
RCV000427319
RCV000427528
RCV000429238
RCV000432840
RCV000432114
RCV000434062
RCV000436873
RCV000438684
RCV000440130
RCV000439934
RCV000442713
RCV000442639
RCV001205860
RCV003463827
RCV004022226
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263624.1:p.Lys93Gln
CA16603047
NM_001276695.3:c.277A>C