Canonical Allele Identifier: PA1139668131
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 936526
ClinVar RCV Id: RCV001205342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Ser60Arg
CA415257547
NM_000117.3:c.178A>C
CA415257553
NM_000117.3:c.180C>A
CA415257554
NM_000117.3:c.180C>G