Canonical Allele Identifier: PA210990
Gene: MAG HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542167.1:p.Cys430Gly
CA210989
NM_080600.3:c.1288T>G