Canonical Allele Identifier: PA325736
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 36030
ClinVar RCV Id: RCV000686102 RCV003103716 RCV003492301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Arg157Gln
CA325734
NM_000117.3:c.470G>A