Canonical Allele Identifier: PA2741906365
Gene: EMX2 HGNC NCBI
ClinVar RCV:
RCV003383290
ClinVar Variation:
2619841
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Amino-acid Alleles

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