ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825609994
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
233951
ClinVar RCV Id:
RCV000214341
RCV000223396
RCV000418173
RCV000418768
RCV000429546
RCV000435180
RCV000440133
RCV000418817
RCV000429913
RCV000423542
RCV000423333
RCV000424469
RCV000433605
RCV000434638
RCV000439338
RCV000435365
RCV000441217
RCV000477355
RCV000785308
RCV001255635
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119587.1:p.Val41Met
CA10577579
NM_001126115.1:c.121G>A