Canonical Allele Identifier: PA111066
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16194
ClinVar RCV Id: RCV000017578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Leu394Arg
CA126262
NM_000821.7:c.1181T>G