Canonical Allele Identifier: PA2741906365
Gene: EMX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2619841
ClinVar RCV Id: RCV003383290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004089.1:p.Ser219Leu
CA5711517
NM_004098.4:c.656C>T