Canonical Allele Identifier: PA2825214573
Gene: MGP HGNC NCBI

Linked Data

ClinVar Variation Id: 432101
ClinVar RCV Id: RCV000497490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000891.2:p.Cys19Tyr
CA384021233
NM_000900.5:c.56G>A