ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA287724
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127814
ClinVar RCV Id:
RCV000115725
RCV000419946
RCV000436926
RCV000419252
RCV000430191
RCV000434251
RCV000442798
RCV000427698
RCV000434917
RCV000443742
RCV000526324
RCV000423543
RCV000424864
RCV000429510
RCV000785334
RCV000435593
RCV000443833
RCV000492788
RCV004019613
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Tyr124Cys
CA000240
NM_001126118.1:c.371A>G