Canonical Allele Identifier: PA1139697801
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 895110
ClinVar RCV Id: RCV001137013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298241.1:p.Lys91Gln
CA347492328
NM_001311312.2:c.271A>C