Canonical Allele Identifier: PA645386480
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 337273
ClinVar RCV Id: RCV000323161 RCV000907563 RCV003910308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Asn177Asp
CA1742108
NM_000821.7:c.529A>G