ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825618550
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376621
ClinVar RCV Id:
RCV000418615
RCV000425759
RCV000428426
RCV000436027
RCV000435616
RCV000436676
RCV000444896
RCV000785451
RCV001301950
RCV002392946
RCV004022222
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Ile216Phe
CA16603041
NM_001126118.1:c.646A>T