Canonical Allele Identifier: PA645472019
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 290157
ClinVar RCV Id: RCV000695175 RCV000396796 RCV000726441 RCV003298348
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Gly156Arg
CA10561623
NM_000117.3:c.466G>C