Canonical Allele Identifier: PA2580104341
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2043011
ClinVar RCV Id: RCV002908367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Arg150Gly
CA415258352
NM_000117.3:c.448A>G