Canonical Allele Identifier: PA645396760
Gene: MGP HGNC NCBI

Linked Data

ClinVar Variation Id: 432101
ClinVar RCV Id: RCV000497490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177768.1:p.Cys19Tyr
CA384021233
NM_001190839.1:c.56G>A