Allele Registry

Canonical Allele Identifier: PA2580507702

Gene: EMID1 HGNC NCBI

ClinVar RCV:

RCV004197144

ClinVar Variation:

2353749

HGVS (amino-acid)	Matching Registered Transcripts
NP_597712.2:p.His289Gln	CA10170588 NM_133455.4:c.867C>G CA411108426 NM_133455.4:c.867C>A