Canonical Allele Identifier: PA915988757
Gene: GEMIN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 715039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056536.2:p.Thr529Ser
CA8262605
NM_015721.3:c.1585A>T
CA397506778
NM_015721.3:c.1586C>G