Canonical Allele Identifier: PA111095
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16195
ClinVar RCV Id: RCV000017579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Trp501Ser
CA126263
NM_000821.7:c.1502G>C