Canonical Allele Identifier: PA645397314
Gene: GALNT12 HGNC NCBI

Linked Data

ClinVar Variation Id: 410594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078918.3:p.Arg9Gly
CA16612696
NM_024642.5:c.25C>G