Canonical Allele Identifier: PA1139668207
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 967061
ClinVar RCV Id: RCV001241881 RCV001828987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Ser196Phe
CA10561642
NM_000117.3:c.587C>T