Canonical Allele Identifier: PA645389498
Gene: COG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705831.1:p.Ala696Val
CA7960795
NM_153603.4:c.2087C>T