Canonical Allele Identifier: PA2573163030
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1373752
ClinVar RCV Id: RCV001877475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Glu146Gly
CA415258305
NM_000117.3:c.437A>G