Canonical Allele Identifier: PA2580119645
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 2175900
ClinVar RCV Id: RCV002582111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Arg498Leu
CA347484974
NM_000821.7:c.1493G>T