ClinGen Allele Registry
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Canonical Allele Identifier:
PA915956929
Gene: CP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
289123
ClinVar RCV:
RCV000260851
RCV001770276
RCV002520097
ClinVar Variation:
343773
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000087.2:p.Ala406Glu
CA2661092
NM_000096.4:c.1217C>A