ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA166963
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
141967
ClinVar RCV Id:
RCV000130712
RCV000478688
RCV000633343
RCV002247510
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119584.1:p.Ala86Thr
CA000088
NM_001126112.3:c.256G>A