Canonical Allele Identifier: PA111042
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16197
ClinVar RCV Id: RCV000017581 RCV003556035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Arg485Pro
CA126264
NM_000821.7:c.1454G>C