Canonical Allele Identifier: PA2573163025
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1470909
ClinVar RCV Id: RCV001964410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Asp137Glu
CA415258186
NM_000117.3:c.411C>A
CA415258188
NM_000117.3:c.411C>G