Canonical Allele Identifier: PA645389440
Gene: COG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 318486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705831.1:p.Ala136Thr
CA7961315
NM_153603.4:c.406G>A