Canonical Allele Identifier: PA2825838046
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16195
ClinVar RCV Id: RCV000017579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Trp444Ser
CA126263
NM_001142269.2:c.1331G>C