ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA121385
Gene: EMD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000011926
RCV000078128
RCV002381248
ClinVar Variation:
11176
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000108.1:p.Gln44Ter