Canonical Allele Identifier: PA131120
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 42272
ClinVar RCV Id: RCV000035105 RCV000770588 RCV002426545 RCV000756071 RCV001085397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Asn91Ser
CA131118
NM_000117.3:c.272A>G