Canonical Allele Identifier: PA2825837978
Gene: GGCX HGNC NCBI
ClinVar RCV:
RCV000017578
ClinVar Variation:
16194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Leu337Arg
CA126262
NM_001142269.2:c.1010T>G