ClinGen Allele Registry
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Canonical Allele Identifier:
PA174206
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000149050
RCV000255749
RCV000418383
RCV000418979
RCV000421625
RCV000422957
RCV000423995
RCV000424505
RCV000429269
RCV000429720
RCV000430374
RCV000431935
RCV000433054
RCV000434273
RCV000436020
RCV000440516
RCV000441726
RCV000444033
RCV000444063
RCV000445061
RCV000492556
RCV000709403
RCV000785456
RCV002288661
ClinVar Variation:
161516
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119589.1:p.Gly134Glu
CA000421
NM_001126117.1:c.401G>A