Canonical Allele Identifier: PA2499228580
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1059971
ClinVar RCV Id: RCV001369340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Asp70Tyr
CA415257627
NM_000117.3:c.208G>T