Canonical Allele Identifier: PA2825837910
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16206
ClinVar RCV Id: RCV000017590 RCV001824572 RCV001851893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Val198Met
CA214957
NM_001142269.2:c.592G>A