Canonical Allele Identifier: PA658654919
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 444835
ClinVar RCV Id: RCV000513465 RCV000701008 RCV001271614 RCV003492086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Val134Met
CA337289975
NM_000117.3:c.400G>A