Canonical Allele Identifier: PA2825228681
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 2233215
ClinVar RCV Id: RCV002747012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Asp89Tyr
CA347492347
NM_000821.7:c.265G>T