Canonical Allele Identifier: PA2580104311
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1794316
ClinVar RCV Id: RCV002453058 RCV003150568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Lys88Asn
CA415257764
NM_000117.3:c.264G>C
CA415257765
NM_000117.3:c.264G>T