Canonical Allele Identifier: PA2825838063
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16200
ClinVar RCV Id: RCV000017584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Gly501Arg
CA214951
NM_001142269.2:c.1501G>A
CA347484571
NM_001142269.2:c.1501G>C