Allele Registry

Canonical Allele Identifier: PA2580558289

Gene: EMB HGNC NCBI

ClinVar RCV:

RCV004176746

ClinVar Variation:

2330270

HGVS (amino-acid)	Matching Registered Transcripts
NP_940851.1:p.Lys321Asn	CA359708209 NM_198449.3:c.963A>T CA359708210 NM_198449.3:c.963A>C