Canonical Allele Identifier: PA2825838022
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 895043
ClinVar RCV Id: RCV001136911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Arg428Cys
CA1741805
NM_001142269.2:c.1282C>T